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Anomalia de Ebstein da válvula tricúspide
ORPHA:1880CID-10 · Q22.5CID-11 · LA87.03OMIM 224700DOENÇA RARA

A malformação de Ebstein é uma anomalia cardíaca congênita rara caracterizada pelo deslocamento rotacional dos folhetos septais e inferiores da válvula tricúspide, de modo que eles fiquem articulados dentro do ventrículo direito, e não como esperado na junção atrioventricular.

Mantido por Agente Raras·Colaborar como especialista →

Introdução

O que você precisa saber de cara

📋

A malformação de Ebstein é uma anomalia cardíaca congênita rara caracterizada pelo deslocamento rotacional dos folhetos septais e inferiores da válvula tricúspide, de modo que eles fiquem articulados dentro do ventrículo direito, e não como esperado na junção atrioventricular.

Publicações científicas
193 artigos
Último publicado: 2026 Apr

Escala de raridade

CLASSIFICAÇÃO ORPHANET · BRASIL 2024
1-9 / 100 000
Ultra-rara
<1/50k
Muito rara
1/20k
Rara
1/10k
Pouco freq.
1/5k
Incomum
1/2k
Prevalência
1.25
Europe
Início
All ages
🏥
SUS: Cobertura mínimaScore: 35%
Centros em: RS, PR, SC, PA, PE +10CID-10: Q22.5
🇧🇷Dados SUS / DATASUS
PROCEDIMENTOS SIGTAP (5)
0202010503
Cariótipo — bandas G, Q ou Rgenetic_test
0202010600
Pesquisa de microdeleções/microduplicações por FISHlab_test
0202010694
Sequenciamento completo do exoma (WES)rehabilitation
0202010260
Dosagem de alfa-fetoproteína
0301070040
Atendimento em reabilitação — doenças raras
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Entender a doença

Do básico ao detalhe, leia no seu ritmo

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Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Partes do corpo afetadas

❤️
Coração
13 sintomas
🫁
Pulmão
2 sintomas
🩸
Sangue
1 sintomas
🧠
Neurológico
1 sintomas

+ 13 sintomas em outras categorias

Características mais comuns

90%prev.
Fadiga
Muito frequente (99-80%)
90%prev.
Nascimento prematuro
Muito frequente (99-80%)
90%prev.
Insuficiência respiratória
Muito frequente (99-80%)
90%prev.
Anomalia de Ebstein da valva tricúspide
Muito frequente (99-80%)
90%prev.
Valva tricúspide imperfurada
Muito frequente (99-80%)
90%prev.
Defeito do septo atrial
Muito frequente (99-80%)
30sintomas
Muito frequente (7)
Frequente (10)
Ocasional (8)
Muito raro (2)
Sem dados (3)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 30 características clínicas mais associadas, ordenadas por frequência.

FadigaFatigue
Muito frequente (99-80%)90%
Nascimento prematuroPremature birth
Muito frequente (99-80%)90%
Insuficiência respiratóriaRespiratory insufficiency
Muito frequente (99-80%)90%
Anomalia de Ebstein da valva tricúspideEbstein anomaly of the tricuspid valve
Muito frequente (99-80%)90%
Valva tricúspide imperfuradaImperforate tricuspid valve
Muito frequente (99-80%)90%

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa1desde 2026
Total histórico193PubMed
Últimos 10 anos200publicações
Pico202445 papers
Linha do tempo
2026Hoje · 2026📈 2024Ano de pico
Publicações por ano (últimos 10 anos)

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

Genes associados

1 gene identificado com associação a esta condição. Padrão de herança: Autosomal dominant, Not applicable.

MYH7Myosin-7Disease-causing germline mutation(s) inTolerante
FUNÇÃO

Myosins are actin-based motor molecules with ATPase activity essential for muscle contraction. Forms regular bipolar thick filaments that, together with actin thin filaments, constitute the fundamental contractile unit of skeletal and cardiac muscle

LOCALIZAÇÃO

Cytoplasm, myofibrilCytoplasm, myofibril, sarcomere

MECANISMO DE DOENÇA

Cardiomyopathy, familial hypertrophic, 1

A hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.

EXPRESSÃO TECIDUAL(Ubíquo)
Coração - Ventrículo esquerdo
4513.7 TPM
Músculo esquelético
3692.8 TPM
Coração - Átrio
592.2 TPM
Pâncreas
5.3 TPM
Hipotálamo
4.9 TPM
OUTRAS DOENÇAS (12)
MYH7-related skeletal myopathymyopathy, myosin storage, autosomal recessivedilated cardiomyopathy 1Scongenital myopathy 7A, myosin storage, autosomal dominant
HGNC:7577UniProt:P12883

Variantes genéticas (ClinVar)

1,439 variantes patogênicas registradas no ClinVar.

🧬 MYH7: NM_000257.4(MYH7):c.1369A>G (p.Ile457Val) ()
🧬 MYH7: NM_000257.4(MYH7):c.1712G>A (p.Gly571Glu) ()
🧬 MYH7: NM_000257.4(MYH7):c.2070G>A (p.Met690Ile) ()
🧬 MYH7: NM_000257.4(MYH7):c.2168G>C (p.Arg723Pro) ()
🧬 MYH7: NM_000257.4(MYH7):c.2629A>G (p.Met877Val) ()
Ver todas no ClinVar

Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

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Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

Pipeline de tratamentos
Pipeline regulatório — de medicamentos já aprovados a drogas em pesquisa exploratória.
1Fase 11
·Pré-clínico3
Medicamentos catalogadosEnsaios clínicos· 0 medicamentos · 4 ensaios
Carregando informações de tratamento...

Onde tratar no SUS

Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)

🇧🇷 Atendimento SUS — Anomalia de Ebstein da válvula tricúspide

Centros de Referência SUS

24 centros habilitados pelo SUS para Anomalia de Ebstein da válvula tricúspide

Centros para Anomalia de Ebstein da válvula tricúspide

Detalhes dos centros

Hospital Universitário Prof. Edgard Santos (HUPES)

R. Dr. Augusto Viana, s/n - Canela, Salvador - BA, 40110-060 · CNES 0003808

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital Infantil Albert Sabin

R. Tertuliano Sales, 544 - Vila União, Fortaleza - CE, 60410-794 · CNES 2407876

Serviço de Referência

Rota
Anomalias CongênitasDeficiência Intelectual

Hospital de Apoio de Brasília (HAB)

AENW 3 Lote A Setor Noroeste - Plano Piloto, Brasília - DF, 70684-831 · CNES 0010456

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Estadual Infantil e Maternidade Alzir Bernardino Alves (HIABA)

Av. Min. Salgado Filho, 918 - Soteco, Vila Velha - ES, 29106-010 · CNES 6631207

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital das Clínicas da UFG

Rua 235 QD. 68 Lote Área, Nº 285, s/nº - Setor Leste Universitário, Goiânia - GO, 74605-050 · CNES 2338424

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital Universitário da UFJF

R. Catulo Breviglieri, Bairro - s/n - Santa Catarina, Juiz de Fora - MG, 36036-110 · CNES 2297442

Atenção Especializada

Rota
Anomalias Congênitas

Hospital das Clínicas da UFMG

Av. Prof. Alfredo Balena, 110 - Santa Efigênia, Belo Horizonte - MG, 30130-100 · CNES 2280167

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário Julio Müller (HUJM)

R. Luis Philippe Pereira Leite, s/n - Alvorada, Cuiabá - MT, 78048-902 · CNES 2726092

Atenção Especializada

Rota
Anomalias Congênitas

Hospital Universitário João de Barros Barreto

R. dos Mundurucus, 4487 - Guamá, Belém - PA, 66073-000 · CNES 2337878

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário Lauro Wanderley (HULW)

R. Tabeliao Estanislau Eloy, 585 - Castelo Branco, João Pessoa - PB, 58050-585 · CNES 0002470

Atenção Especializada

Rota
Anomalias Congênitas

Instituto de Medicina Integral Prof. Fernando Figueira (IMIP)

R. dos Coelhos, 300 - Boa Vista, Recife - PE, 50070-902 · CNES 0000647

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Pequeno Príncipe

R. Des. Motta, 1070 - Água Verde, Curitiba - PR, 80250-060 · CNES 3143805

Serviço de Referência

Rota
Anomalias CongênitasDeficiência Intelectual

Hospital Universitário Regional de Maringá (HUM)

Av. Mandacaru, 1590 - Parque das Laranjeiras, Maringá - PR, 87083-240 · CNES 2216108

Atenção Especializada

Rota
Anomalias Congênitas

Hospital de Clínicas da UFPR

R. Gen. Carneiro, 181 - Alto da Glória, Curitiba - PR, 80060-900 · CNES 2364980

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário Pedro Ernesto (HUPE-UERJ)

Blvd. 28 de Setembro, 77 - Vila Isabel, Rio de Janeiro - RJ, 20551-030 · CNES 2280221

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira (IFF/Fiocruz)

Av. Rui Barbosa, 716 - Flamengo, Rio de Janeiro - RJ, 22250-020 · CNES 2269988

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital São Lucas da PUCRS

Av. Ipiranga, 6690 - Jardim Botânico, Porto Alegre - RS, 90610-000 · CNES 2232928

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital de Clínicas de Porto Alegre (HCPA)

Rua Ramiro Barcelos, 2350 Bloco A - Av. Protásio Alves, 211 - Bloco B e C - Santa Cecília, Porto Alegre - RS, 90035-903 · CNES 2237601

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário da UFSC (HU-UFSC)

R. Profa. Maria Flora Pausewang - Trindade, Florianópolis - SC, 88036-800 · CNES 2560356

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital das Clínicas da FMUSP

R. Dr. Ovídio Pires de Campos, 225 - Cerqueira César, São Paulo - SP, 05403-010 · CNES 2077485

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital de Base de São José do Rio Preto

Av. Brg. Faria Lima, 5544 - Vila Sao Jose, São José do Rio Preto - SP, 15090-000 · CNES 2079798

Atenção Especializada

Rota
Anomalias Congênitas

Hospital de Clínicas da UNICAMP

R. Vital Brasil, 251 - Cidade Universitária, Campinas - SP, 13083-888 · CNES 2748223

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital de Clínicas de Ribeirão Preto (HCRP-USP)

R. Ten. Catão Roxo, 3900 - Vila Monte Alegre, Ribeirão Preto - SP, 14015-010 · CNES 2082187

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

UNIFESP / Hospital São Paulo

R. Napoleão de Barros, 715 - Vila Clementino, São Paulo - SP, 04024-002 · CNES 2688689

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo
Sobre os centros SUS: Estes centros são habilitados pelo Ministério da Saúde como Serviços de Referência em Doenças Raras ou Serviços de Atenção Especializada. O atendimento é pelo SUS, com encaminhamento da rede de atenção básica.

Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.

Pesquisa ativa

Ensaios clínicos abertos e novidades científicas recentes

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Publicações mais relevantes

📖Melhor nível de evidência: Revisão
Timeline de publicações
13 papers (10 anos)
#1

Septal Leaflet Augmentation During the Da Silva Cone Repair: Valvar Function and Anatomical Features Compared to Non-Patch Repair.

The Journal of thoracic and cardiovascular surgery2026 Mar 10

To evaluate outcomes of Da Silva Cone repair (CR) using autologous pericardial patch for septal leaflet augmentation in Ebstein's anomaly (EA) and identify tricuspid valve (TV) morphology associated with patch use. A single-site retrospective study included patients undergoing CR for EA from Jan 2016-Nov 2024. Patients with prior Starnes procedure or TV surgery were excluded. Patients were categorized into patch and non-patch groups. The primary outcome was TV function (stenosis or regurgitation) at latest follow-up with a secondary composite outcome including re-operation or >moderate residual tricuspid regurgitation (TR). Adjusted regression analyses identified factors associated with outcomes and patch augmentation. Of 134 patients identified, 108 were included (50 patch, 58 non-patch). Patch patients were older (13.1 vs. 6.9 years, p=0.04). TR improved from ≥moderate in 78.7% pre-CR to ≤mild in 79.0% at follow-up. TV function and follow-up TV-related re-operation rates (6.0% vs. 1.7%) were comparable between groups (p>0.05) with a median follow-up of 1.1 years (IQR 0.6-3.2). Intraoperative factors associated with patch use were multiple TV orifices (OR=4.24, 95%CI: 1.59-11.27, p<0.01), absence of severe inferior leaflet displacement (OR=3.24, 95%CI: 1.11-9.47, p=0.03), and absence of extreme TV rotation (OR=3.19, 95%CI: 1.21-8.41, p=0.02). Autologous pericardial patch augmentation of the septal leaflet provides comparable early TV function and freedom from re-operation, making it an effective complement during CR.

#2

Biventricular Repair in Symptomatic Neonates with Ebstein Anomaly: 25-30 years of follow-up.

The Journal of thoracic and cardiovascular surgery2026 Mar 02

The first report of successful biventricular repairs of Ebstein Anomaly in the severely symptomatic neonate was published in 2000 and 2002. We sought to ascertain the long-term follow-up of the survivors over the ensuing 25-31 years. Eight consecutive neonates (n=6) and young infants (n=2) underwent primary biventricular repair of Ebstein anomaly between April 1994 and March 2001 by one surgeon at the Children's Hospital of Oklahoma. Complete follow-up of all patients was achieved in August 2025 by personal contact with the patients, their parents and/or their cardiologists. All patients gave consent to their data to be included in this review. Three neonates had associated pulmonary atresia and two had functional pulmonary atresia, one with circular shunt and cardiogenic shock. Two had an associated ventricular septal defect. One 2.5-month-old ventilator-dependent neonate had undergone a Starnes' single ventricle palliation elsewhere. All patients had severe tricuspid regurgitation and Great Ormond Street Echocardiography (GOSE) scores grade III (n=2) or IV (N=6). Three neonates had symptomatic tachyarrhythmias prior to surgery. Simplified biventricular repair was done in all 8 patients and all associated cardiac defects were repaired. There was one hospital death (1/8, 12.5%) in a 2.1kg neonate with anatomical pulmonary atresia. All 7 hospital survivors are currently alive and well. The transplant-free survival at 25-31-year follow-up of the hospital survivors (n=7) was 100%. The reoperation-free survival was 75% at 15 years and 43% at 25 years follow-up. No patient developed tachyarrhythmias postoperatively; one patient developed atrial fibrillation at 22 years follow-up. Biventricular repair in symptomatic neonates with Ebstein anomaly is feasible and associated with excellent long-term outcomes. Re-repair or replacement of the tricuspid valve can be anticipated over a follow-up period of 15-30 years.

#3

Risk factors for morbidity and mortality in Ebstein's anomaly: a registry-based study of 398 patients.

Clinical research in cardiology : official journal of the German Cardiac Society2026 Mar 04

To investigate the long-term outcomes and risk factors for morbidity and mortality in patients with Ebstein's anomaly, including the effects of type and timing of valve surgery. For this retrospective, record-based study, all patients with Ebstein's anomaly enrolled in the German National Register for Congenital Heart Defects up to June 2021 were eligible for inclusion. Non-surgical patients (n = 194/49% of 398 patients) had less tricuspid valve regurgitation (p < 0.001) and heart failure symptoms (p < 0.001) than surgical patients (n = 204/51%). Postoperative survival at 10, 20, and 30 years was 97%, 93%, and 80%. Eighty-one (40%) patients underwent multiple surgeries. Re-operation rates were lowest in patients with first valve surgery during adolescence (p = 0.0076). Postoperative NYHA class > I was more frequent with surgery delayed to older age (p < 0.001). Initial corrective surgery was complicated by complete atrioventricular block (CAVB) in 17 (9%) of patients. CAVB was more likely with older age (p = 0.001), and tricuspid valve replacement compared to reconstruction (p = 0.029). CAVB was associated with all-cause death (p < 0.001). Cone reconstruction reduced the risk of CAVB (p = 0.008) and tricuspid valve regurgitation (p < 0.001) compared to monocusp reconstruction. This registry-based study of Ebstein's anomaly corroborates good surgical long-term results, while re-operation rates remain high. Patients operated before adolescence were at the highest risk of re-operation, while older age at the time of the first surgery increased the risk of CAVB. The cone reconstruction was associated with improved tricuspid valve function and a lower risk of CAVB compared to monocusp reconstructions. Choosing an optimal time window for surgery and use of the cone reconstruction may therefore further improve outcomes.

#4

Changing Course-Starnes Takedown in High-Risk Children and Review of the Current Literature.

Pediatric cardiology2026 Feb 14

Neonates with Ebstein anomaly or severe tricuspid valve dysplasia represent a high-risk patient cohort. The modified Starnes procedure was historically performed for cases incompatible with biventricular (BV) repair, leading them towards single-ventricle palliation. However, in recent years, a paradigm shift has emerged in which the Starnes procedure in the acute setting can provide a means for right ventricular (RV) rehabilitation, by providing relief of RV volume overload and time for recovery of RV function, thus serving as a bridge to subsequent one and a half ventricle or BV repair. Herein, we present two cases at our institution of successful transition to BV repair after the Starnes procedure, despite an initially failed index BV repair as a neonate. Both patients presented with severe tricuspid valve dysplasia. The first patient underwent Starnes procedure at 10 days of life and takedown at 4 years of age after bilateral cavopulmonary shunt (BCPS) failure from recurrent bilateral pulmonary artery stenoses. The 2nd patient received Starnes at 4 months of age and successfully underwent takedown at 18mo after being deemed an unsuitable candidate for BCPS. Improvement in RV function was noted throughout the Starnes course. By providing our center's experience in the context of other case reports and series of BV conversion post-Starnes procedure, summarizing clinical and surgical considerations advocated in recent guidelines, and highlighting the topical areas of management that remain to be elucidated, we hope this discussion can lead to appropriate adoption of this new treatment strategy.

#5

Use of right atrial wall to repair severely dysplastic tricuspid valve in an infant with Ebstein's anomaly.

Multimedia manual of cardiothoracic surgery : MMCTS2026 Feb 02

The management of infants with Ebstein's anomaly is challenging and requires complex involvement of the multidisciplinary team. Surgical repair technique is dependent on the degree of tricuspid leaflet dysfunction and the decision to undergo univentricular or biventricular repair. Patients with a severely dysplastic tricuspid valve are less suited to a cone repair alone and require leaflet reconstruction. Currently used patch materials include autologous untreated pericardium and treated pericardium, with limitations such as unpredictable shrinkage and no growth potential, respectively. To overcome these challenges, we used living autologous wall of the right atrium to reconstruct the tricuspid valve leaflets in a 1-year-old girl with Ebstein's anomaly and a severely dysplastic tricuspid valve.

Publicações recentes

Ver todas no PubMed

📚 EuropePMC3 artigos no totalmostrando 198

2026

Left bundle branch area pacing from the functional right ventricle in Ebstein's anomaly with atrioventricular block.

HeartRhythm case reports
2026

Septal Leaflet Augmentation During the Da Silva Cone Repair: Valvar Function and Anatomical Features Compared to Non-Patch Repair.

The Journal of thoracic and cardiovascular surgery
2026

Biventricular Repair in Symptomatic Neonates with Ebstein Anomaly: 25-30 years of follow-up.

The Journal of thoracic and cardiovascular surgery
2026

Risk factors for morbidity and mortality in Ebstein's anomaly: a registry-based study of 398 patients.

Clinical research in cardiology : official journal of the German Cardiac Society
2026

Changing Course-Starnes Takedown in High-Risk Children and Review of the Current Literature.

Pediatric cardiology
2026

Use of right atrial wall to repair severely dysplastic tricuspid valve in an infant with Ebstein's anomaly.

Multimedia manual of cardiothoracic surgery : MMCTS
2025

Clinical and Imaging Predictors of Poor Prognosis in Ebstein Anomaly.

CJC pediatric and congenital heart disease
2026

Timely surgical intervention and risk stratification in patients with Ebstein anomaly: a 20-year retrospective cohort study.

International journal of surgery (London, England)
2025

Systemic atrioventricular valve replacement due to a supravalvular stenosing ring and ebsteinoid tricuspid valve in a patient with congenitally corrected transposition of the great arteries: a case report.

Archivos peruanos de cardiologia y cirugia cardiovascular
2026

Biventricular remodeling and function after Cone repair of Ebstein Anomaly: A review.

International journal of cardiology. Congenital heart disease
2026

Transcatheter Tricuspid Valve-in-Valve Replacement in a Patient with Ebstein Anomaly.

Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir
2026

Cardiovascular Profile Score and Perinatal Survival Among Fetuses With Ebstein's Anomaly or Tricuspid Valve Dysplasia: A Multi-Center Retrospective Cohort Study.

Prenatal diagnosis
2026

Anatomical severity of Ebstein's anomaly: a quantitative analysis based on cardiovascular MRI.

Open heart
2025

First surgical epicardial implantation of an extravascular implantable cardioverter-defibrillator lead for Ebstein anomaly in the United States.

HeartRhythm case reports
2025

Primary Tricuspid Regurgitation: From Neglect to Clinical Relevance.

Journal of personalized medicine
2025

Catheter ablation of macro-reentrant atrial tachycardia in adults with Ebstein anomaly: A narrative review.

Heart rhythm O2
2025

Perioperative management of a woman with Ebstein's anomaly undergoing caesarean section.

BMJ case reports
2026

Versatility of the right atrial wall for tricuspid valve repair in children with Ebstein anomaly.

The Journal of thoracic and cardiovascular surgery
2025

Cone repair and right ventricular resection in an adult patient with Ebstein's anomaly.

Multimedia manual of cardiothoracic surgery : MMCTS
2026

Ebstein Anomaly and the Range of Right-Sided Heart Defects.

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
2025

Arrhythmias in Congenital Heart Disease: Ebstein Anomaly.

Cardiac electrophysiology clinics
2025

First Confirmed Case of Leadless Pacemaker Insertion via Bidirectional Glenn Shunt in Ebstein's Anomaly: A Novel Approach to Pacing Challenges.

Journal of cardiovascular electrophysiology
2025

Echocardiographic characteristics of 14 cases with uncommon manifestation of Ebstein anomaly in the fetus: a case series report.

Archives of gynecology and obstetrics
2025

A multifaceted clinical portrait of Ebstein's anomaly: a case series.

European heart journal. Case reports
2026

Surgically Treated Giant Right Atrium in Isolated Severe Tricuspid Regurgitation.

World journal for pediatric &amp; congenital heart surgery
2025

Outcomes of the Fontan operation in patients with Ebstein anomaly: An Australia and New Zealand Fontan registry study.

JTCVS open
2025

Surgical Management of Ebstein's Anomaly in Elderly Patients: A Report of Two Cases.

Cureus
2025

Ebstein Anomaly and Atrial Conduction: Big Does Not Mean Bad.

Circulation. Arrhythmia and electrophysiology
2025

Interventricular septal hematoma following cone repair for Ebstein's anomaly.

Indian journal of thoracic and cardiovascular surgery
2025

Ebstein anomaly update: the evolution of care and the revolution of surgical strategy.

Expert review of cardiovascular therapy
2025

Fetal Conduction Disease and Arrhythmia in Ebstein's Anomaly and Tricuspid Valve Dysplasia Assessed by Fetal Magnetocardiography.

Journal of the American Heart Association
2025

Mid-Term Recovery of Right Ventricular Function and Improvement of Left Ventricular Function After Da Silva Cone Procedure for Ebstein Anomaly.

Journal of cardiovascular development and disease
2025

A Staged Biventricular Approach Combining the Starnes and Cone Procedures in Ebstein's Anomaly: A Case Report and Literature Review.

Children (Basel, Switzerland)
2025

CARTO UNIVU-Guided Micra Implantation in Ebstein Anomaly.

JACC. Case reports
2025

Biventricular remodeling after cone repair in Ebstein anomaly: magnetic resonance imaging data analysis.

Journal of thoracic disease
2024

Lithium-induced Ebstein's Anomaly.

Heart views : the official journal of the Gulf Heart Association
2025

Surgical trends and outcomes of neonatal Ebstein's anomaly: Multi-institutional study.

The Journal of thoracic and cardiovascular surgery
2025

Ebstein Repair in a High-Altitude Setting ≥2,500 m: First Experience from Bolivia.

The Thoracic and cardiovascular surgeon
2025

Cone reconstruction after carpentier repair in ebstein anomaly: yes we can!

Journal of cardiothoracic surgery
2025

[Echocardiographic characteristics and prognostic evaluation of Ebstein anomaly in fetuses].

Zhonghua er ke za zhi = Chinese journal of pediatrics
2025

Staged Treatment for Critically Ill Neonates With Ebstein Anomaly: Cone Repair After Starnes Procedure.

Seminars in thoracic and cardiovascular surgery. Pediatric cardiac surgery annual
2025

Exercise Performance and Right Ventricular Remodeling After the Cone Repair in Patients With Different Severity of Ebstein Anomaly.

The Annals of thoracic surgery
2025

The American Association for Thoracic Surgery (AATS) 2025 Expert Consensus Document: Management of Ebstein anomaly in children and adults.

The Journal of thoracic and cardiovascular surgery
2025

Practical approach to using cardiac magnetic resonance imaging for pre-surgical planning in complex paediatric congenital heart disease.

Pediatric radiology
2025

A dual-chamber leadless pacemaker implantation across percutaneous tricuspid valve-in-valve prosthesis in a patient with Ebstein anomaly.

HeartRhythm case reports
2024

SUCCESSFUL ABLATION OF CONCEALED ACCESSORY PATHWAY MEDIATED SUPRAVENTRICULAR TACHYCARDIA IN A 5-YEAR-OLD CHILD WITH EBSTEIN ANOMALY.

Acta clinica Croatica
2025

Left Bundle Branch Pacing in a Pediatric Patient With Tricuspid Valve Replacement for a Complex Ebstein Anomaly.

Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc
2025

Presentation of Asymptomatic Ebstein's Anomaly: A Case Report.

Cureus
2025

Ebstein's anomaly in children and young adults: clinical features, arrhythmia, surgical management, and factors affecting arrhythmia and mortality.

Cardiology in the young
2024

Intraoperative Hemodynamic Instability in a Patient With Ebstein's Anomaly Complicated With Eisenmenger Syndrome.

Case reports in cardiology
2025

Circular Shunt: A Loop Not to Be Ignored.

Journal of cardiothoracic and vascular anesthesia
2024

Complete surgical correction of tetralogy of Fallot with Ebstein's anomaly.

Annals of pediatric cardiology
2024

Tricuspid valve septal displacement cutoff value for mortality risk following biventricular repair in Ebstein anomaly.

Annals of pediatric cardiology
2024

Surgical strategies in Ebstein anomaly: 28 years' experience in a pediatric hospital.

Archivos de cardiologia de Mexico
2024

Electrophysiologic Considerations in Adult Patients with Ebstein's Anomaly.

Journal of personalized medicine
2024

Case report of Ebstein's anomaly in a young female.

SAGE open medical case reports
2024

Primary cardiac myxofibrosarcoma in a patient with Ebstein's anomaly: First reported case.

International journal of surgery case reports
2025

Combined Norwood and Modified Left-Sided Starnes Procedures for Congenitally Corrected Transposition of the Great Arteries.

World journal for pediatric &amp; congenital heart surgery
2024

Ebstein's Anomaly in a Young Nigerian Lady.

West African journal of medicine
2024

Single-chamber atrial pacing + Micra AV implantation: A case report.

Medicine
2024

Diagnosis of Congenital Heart Disease in Adulthood: How Often, How Relevant?

The American journal of cardiology
2024

A case report of Ebstein's anomaly-Gerbode defect dyad: is there room for another anomaly in the same patient?

European heart journal. Case reports
2024

Ebstein Anomaly Successfully Treated With Levosimendan Postoperatively in a 60-Year-Old Female: A Case Report.

Cureus
2024

Preliminary Study of a Degenerated Tricuspid Bioprosthetic Valve Implanted via Transcatheter Valve-in-Valve Implantation Guided by 3-Dimensional Printing.

CJC open
2024

From ECG to Imaging: Challenges in the Diagnosis of Adult Congenital Heart Diseases.

Journal of clinical medicine
2025

The cone repair allows right ventricle rehabilitation with excellent tricuspid valve function following the Starnes procedure.

The Journal of thoracic and cardiovascular surgery
2025

Large Right Atrial Size on Cardiac MRI is Associated with Post-operative Right Ventricular Dysfunction After the Cone Operation for Ebstein Anomaly.

Pediatric cardiology
2025

Assessing Left Ventricular Pathology in Patients with Ebstein Anomaly Using Cardiovascular Magnetic Resonance: Looking Past the Right Heart.

Pediatric cardiology
2024

Molecular Pathways and Animal Models of Ebstein's Anomaly.

Advances in experimental medicine and biology
2024

Human Genetics of Ebstein Anomaly.

Advances in experimental medicine and biology
2024

Clinical Presentation and Therapy of Ebstein Anomaly.

Advances in experimental medicine and biology
2025

Biventricular function after Ebstein anomaly repair from a single-center echocardiography study.

Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese
2024

Uncommon manifestation of Ebstein anomaly: A case report of apical displacement involving all tricuspid valve leaflets.

Clinical case reports
2024

Management of Ebstein Anomaly in the Current Era: The Story of One Fetus and the Collaboration of Many-A Case Report.

Journal of cardiovascular development and disease
2024

The Connection Between Anatomical Substrate and Clinical Severity in Fetal Ebstein Anomaly.

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
2024

Heart Transplantation for Ebstein Anomaly due to Late Surgical Presentation.

World journal for pediatric &amp; congenital heart surgery
2024

[Comment on the firsts insights of the arterial hypertension study in México (RIHTA): are we doing things right?].

Archivos de cardiologia de Mexico
2024

Ebstein's Anomaly of the Tricuspid Valve.

Rhode Island medical journal (2013)
2024

The American Association for Thoracic Surgery (AATS) 2024 expert consensus document: Management of neonates and infants with Ebstein anomaly.

The Journal of thoracic and cardiovascular surgery
2024

Perinatal outcomes following early prenatal diagnosis: insights from a single-center experience with Ebstein anomaly and tricuspid valve dysplasia.

Archives of gynecology and obstetrics
2024

Study on the correlation between retrograde ductus arteriosus flow and right ventricular function evaluated by Z-score of tricuspid annular plane systolic excursion in fetuses with Ebstein anomaly.

Journal of clinical ultrasound : JCU
2024

Paradoxical septic embolism in an Ebstein's anomaly patient leading to brain abscess: A case report.

Journal of cardiology cases
2024

Ebstein's Anomaly of the Tricuspid Valve, Mitral Valve Prolapse and Left Ventricular Non-Compaction: A Triple Trouble.

Heart, lung &amp; circulation
2024

Ebstein's anomaly: an electrophysiological perspective.

Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing
2024

Surgical Management of Ebstein Anomaly: The Australia and New Zealand Experience.

World journal for pediatric &amp; congenital heart surgery
2023

Discussion to: Outcomes of surgical management of Ebstein anomaly and tricuspid valve dysplasia in critically ill neonates and infants.

JTCVS open
2023

Outcomes of surgical management of Ebstein anomaly and tricuspid valve dysplasia in critically ill neonates and infants.

JTCVS open
2024

Long-Term Outcomes of Modified Cone Reconstruction for Ebstein's Anomaly in Pediatric Patients in a Single Center.

Korean circulation journal
2024

Atrial Fibrillation Ablation in Congenital Heart Disease: Therapeutic Challenges and Future Perspectives.

Journal of the American Heart Association
2024

Prenatal sonographic findings of prominent fetal tricuspid annulus: A case report.

Radiology case reports
2023

Distal His bundle pacing in a patient with surgically corrected complex Ebstein anomaly and symptomatic second-degree atrioventricular block: a case report.

European heart journal. Case reports
2025

Using DaSilva Cone Operation to Establish 1.5 or 2 Ventricle Circulation After Initial Single Ventricle Palliation with Starnes Procedure.

Pediatric cardiology
2024

Strategy and technique for surgical treatment of Ebstein's anomaly.

Chinese medical journal
2024

Ventricular-Ventricular Interactions in Critically Ill Infants with Ebstein Anomaly or Dysplasia of the Tricuspid Valve: Time to Remember the Forgotten Left Ventricle.

Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography
2023

An incidental finding of a right atrial myxoma with undiagnosed Ebstein anomaly: a case report.

European heart journal. Case reports
2024

Cardiac Catheterization in Adults with Ebstein Anomaly: Pathophysiologic Insights Regarding Surgical Repair and Prognosis.

Pediatric cardiology
2024

Impact of Neonatal Intervention on Left Ventricular Performance in Ebstein's Anomaly and Tricuspid Valve Dysplasia.

Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography
2024

Rare loss-of-function variants in matrisome genes are enriched in Ebstein's anomaly.

HGG advances
2024

Ebstein anomaly with severe tricuspid valve regurgitation: An unusual case of an 84-year natural course.

Kardiologia polska
2023

Long-term Outcome of Simultaneous Transcatheter Pulmonary and Tricuspid Valve-in-Valve Implantation in Ebstein Malformation With Pulmonary Insufficiency.

CJC pediatric and congenital heart disease
2024

Commentary: Ebstein anomaly with circular shunt-round and round we go but not necessarily very fast.

The Journal of thoracic and cardiovascular surgery
2023

Intraoperative Transesophageal Echocardiography Evaluation of Tricuspid Valve Re-repair for Ebstein's Anomaly.

Cureus
2024

Significantly elevated hepatic extracellular volume in adult patients with a Fontan circulation and its correlation with impaired functional capacity.

The international journal of cardiovascular imaging
2024

Transplacental non-steroidal anti-inflammatory drugs versus expectant management in fetal Ebstein anomaly with circular shunt: Systematic review and meta-analysis.

Prenatal diagnosis
2023

The Academic Impact of Congenital Heart Surgeons' Society (CHSS) Studies.

World journal for pediatric &amp; congenital heart surgery
2023

Transcatheter thrombectomy of acute pulmonary embolism in an adult Fontan patient: a case report.

European heart journal. Case reports
2023

Heterozygous nonsense variants in laminin subunit 3α resulting in Ebstein's anomaly.

HGG advances
2023

The concept of cone creation to treat isolated tricuspid valve dysplasia and the case of a double-orifice tricuspid valve.

JTCVS techniques
2023

Cone repair after tricuspid valve replacement in Ebstein anomaly.

JTCVS techniques
2023

Pregnancy outcomes in women with Ebstein's anomaly: data from the Registry of Pregnancy And Cardiac disease (ROPAC).

Open heart
2023

Ebstein Anomaly: More Than Just a Tricuspid Valve Issue.

Journal of the American College of Cardiology
2023

Echocardiographic Parameters for Risk Prediction in Borderline Right Ventricle: Review with Special Emphasis on Pulmonary Atresia with Intact Ventricular Septum and Critical Pulmonary Stenosis.

Journal of clinical medicine
2023

Tricuspid cleft or tetracuspid valve? Usefulness of three-dimensional echocardiogram in the assessment of isolated tricuspid regurgitation in pediatrics.

Echocardiography (Mount Kisco, N.Y.)
2023

Comparative outcomes and risk analysis after cone repair or tricuspid valve replacement for Ebstein's anomaly.

JTCVS open
2023

Outcomes after implantation of right-sided mechanical valve prostheses in congenital heart disease.

Heart (British Cardiac Society)
2023

A multidisciplinary approach to re-intervention in an Ebstein patient: a case report.

European heart journal. Case reports
2023

Permanent pacemaker implantation in post one-and-a-half ventricle repair with tricuspid valve replacement in Ebstein anomaly: An innovative technique.

Pacing and clinical electrophysiology : PACE
2023

Peripartum anesthetic management in patients with Ebstein anomaly: a case series.

Proceedings (Baylor University. Medical Center)
2023

Long-term clinical outcomes of tricuspid valve replacement using bovine versus porcine valves: a nationwide population-based study.

European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery
2023

Severe form of Ebstein's anomaly associated with ventricular septal defect.

General thoracic and cardiovascular surgery cases
2023

Percutaneous Mechanical Circulatory Support as a Bridge to Transplantation in Ebstein Anomaly.

Mayo Clinic proceedings
2023

Surgical experience in adults with Ebstein's anomaly: Long-term results.

Cardiovascular journal of Africa
2023

Neurological, Extracardiac, and Cardiac Manifestations of Ebstein's Anomaly Along With its Genetics, Diagnostic Techniques, Treatment Updates, and the Future Ahead.

Cureus
2023

Early spontaneous closure of large arterial ducts in two term neonates with Ebstein anomaly after failed attempts of transcatheter closure.

Cardiology in the young
2024

Early and long-term outcomes of bioprosthetic versus mechanical tricuspid valve replacement: A nationwide population-based study.

The Journal of thoracic and cardiovascular surgery
2023

Treating Supraventricular Tachycardia With Amiodarone in a Patient With Ebstein's Anomaly.

Cureus
2023

Contemporary Early Postoperative Cone Repair Outcomes for Patients With Ebstein Anomaly.

Mayo Clinic proceedings
2023

Percutaneous Closure of Paravalvular Leak After Tricuspid Valve Replacement for Ebstein's Anomaly.

Texas Heart Institute journal
2022

[Atypical chest pain revealing an asymptomatic Ebstein´s anomaly: case report].

The Pan African medical journal
2022

Ebstein's anomaly in a French bulldog.

Veterinary research forum : an international quarterly journal
2022

Tailored strategy to match anatomy and physiology with intervention can improve outcomes of symptomatic neonates with Ebstein anomaly.

JTCVS open
2022

Ebstein's anomaly with pericardial effusion in a 55-year-old lady: A case report.

Annals of medicine and surgery (2012)
2022

Does the right ventricle size influence the left ventricle size and function in children with Ebstein anomaly?

Echocardiography (Mount Kisco, N.Y.)
2023

Sequential percutaneous tricuspid and pulmonary valve implantation in a young child operated previously for Ebstein Anomaly.

Cardiology in the young
2023

Prognostic implications of atrial fibrillation in adults with Ebstein anomaly.

Heart (British Cardiac Society)
2023

Cardiac remodeling after tricuspid valve repair in Ebstein's anomaly: a magnetic resonance study.

European radiology
2023

Late-gestation prediction of outcome in tricuspid valve dysplasia and Ebstein's anomaly using fetal tricuspid regurgitation waveform analysis.

Ultrasound in obstetrics &amp; gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
2022

Ebstein's Anomaly: How to Identify Intracardiac Structures When Electrical Signals Do Not Match the Anatomy.

The Journal of innovations in cardiac rhythm management
2023

Multimodality Imaging in Ebstein Anomaly.

Pediatric cardiology
2022

The Use of Feature Tracking Technique for the Quantification of Ventricular Strain Pattern in Patients with Ebstein's Anomaly: A Case-Control Study.

Iranian journal of medical sciences
2022

Diagnosis and treatment of congenital tricuspid valve malformation in a case of monozygotic twins.

Journal of cardiothoracic surgery
2022

[Ebstein's anomaly with ventricular preexcitation in an adult patient].

Revista medica del Instituto Mexicano del Seguro Social
2022

Detection of early signs of right ventricular systolic impairment in unoperated Ebstein's anomaly by cardiac magnetic resonance feature tracking.

Cardiovascular diagnosis and therapy
2022

Cardiac Implantable Electronic Devices in Ebstein Anomaly: Management and Outcomes.

Circulation. Arrhythmia and electrophysiology
2022

Starr-Edwards tricuspid valve in a patient with Ebstein anomaly: older than half of the century and still functioning well.

European heart journal
2022

Persistent left superior vena cava in a 29-year-old lady with Ebstein's anomaly and complete heart block. A case report and literature review.

Annals of medicine and surgery (2012)
2022

Treatment of Severe Fetal Ebstein's Anomaly with Prenatal Nonsteroidal Anti-Inflammatory Therapy.

Fetal diagnosis and therapy
2023

Comprehensive Evaluation of Pediatric Patients with Ebstein Anomaly Requires Both Echocardiography and Cardiac Magnetic Resonance Imaging.

Pediatric cardiology
2021

Report of persistent left superior vena cava associated with Ebstein's anomaly of tricuspid valve.

ARYA atherosclerosis
2022

Transcatheter Systemic AV Valve-in-Valve Implantation in a Patient With LTGA and Ebstein Anomaly.

JACC. Case reports
2022

Moyamoya Disease Complicating Ebstein's Anomaly.

Internal medicine (Tokyo, Japan)
2022

Implantation of a leadless pacemaker in a patient with mechanical tricuspid valve.

HeartRhythm case reports
2022

Ebstein's Anomaly: From Fetus to Adult-Literature Review and Pathway for Patient Care.

Pediatric cardiology
2022

A Systematic Review of Ebstein's Anomaly with Left Ventricular Noncompaction.

Journal of cardiovascular development and disease
2022

Successful Radiofrequency Ablation of the Right Lateral Accessory Pathway with Modified Carpentier Reconstruction Surgery in a Patient with Ebstein Anomaly Concomitant of Secundum Atrial Septal Defect, Atrial Fibrillation, and Wolff-Parkinson-White Syndrome.

Case reports in vascular medicine
2022

Surgical treatment of tricuspid valve dysplasia in children.

European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery
2022

New trend: Surgical correction of Ebstein's anomaly using modified cone repair and a combination of different techniques.

Journal of cardiac surgery
2022

Displacement of all three leaflets of tricuspid valve: A rare variant of Ebstein anomaly.

Clinical case reports
2022

[Successful Surgical Repair for Adult Ebstein Disease Using Cone Reconstruction Combined with One and a Half Ventricle Repair].

Kyobu geka. The Japanese journal of thoracic surgery
2022

The Mid-Term Outcomes of Cone Repair or Replacement of Tricuspid Valve in Patients with Ebstein's Anomaly: Our Experience.

The heart surgery forum
2022

Cardiac MRI predictors of right ventricular dysfunction after the Da Silva cone operation for Ebstein's anomaly.

International journal of cardiology. Congenital heart disease
2022

Left Ventricular Dysfunction in Neonatal Ebstein's Anomaly and Tricuspid Valve Dysplasia.

Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography
2021

Narrative review of Ebstein's anomaly beyond childhood: Imaging, surgery, and future perspectives.

Cardiovascular diagnosis and therapy
2022

Dual atrial rhythms: a case report of an unusual cause of pacemaker syndrome.

European heart journal. Case reports
2022

Impact of fetal haemodynamics on surgical and neurodevelopmental outcomes in patients with Ebstein anomaly and tricuspid valve dysplasia.

Cardiology in the young
2021

Acute Right Ventricular Reshaping After TriClip in Ebstein's-Like Anomaly Assessed by Multimodality Imaging.

The Journal of invasive cardiology
2022

A case of redo tricuspid valve repair after neonatal cone operation for Ebstein's anomaly.

General thoracic and cardiovascular surgery
2021

Ebstein Anomaly and Right Aortic Arch in Patient with Charge Syndrome.

Medicina (Kaunas, Lithuania)
2021

Transcatheter tricuspid valve-in-valve implantation for degenerative surgical bio-prosthesis using SAPIEN 3: A case series.

Clinical case reports
2021

Modified Starnes procedure as a bridge to 2-ventricle repair in neonatal Ebstein's anomaly: A paradigm shift.

Multimedia manual of cardiothoracic surgery : MMCTS
2021

Successful One-and-a-Half Ventricle Repair of Right Ventricle Dysfunction Due to Lymphoblastic Leukemia Treatment in a Patient with Restrictive Cardiomyopathy.

The American journal of case reports
2021

Ebstein's Anomaly, Left Ventricular Noncompaction and Gerbode-Like Defect Triad (Fetal Diagnosis and Neonatal Course).

Case reports in pediatrics
2021

Imaging for Transcatheter Edge-to-Edge Repair for Tricuspid Regurgitation in Ebstein Anomaly.

Circulation. Cardiovascular imaging
2022

The Association of Pulmonary Flow Characteristics With Cardiac Function in Tricuspid Valve Malformation Fetuses: Study With Two-Dimensional Speckle Tracking Echocardiography.

Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine
2022

Improved Tricuspid Valve Function, Preload Recruitment and Ventricular Efficiency During Submaximal Exercise in Patients with Unoperated Ebstein's Anomaly: An MRI Study.

Journal of magnetic resonance imaging : JMRI
2022

Case Report of a 33-year-old with Ebstein malformation of tricuspid valve and hypertrophic cardiomyopathy.

Cardiology in the young
2021

Cone Reconstruction for Ebstein Anomaly: Ventricular Remodeling and Preliminary Impact of Stem Cell Therapy.

Mayo Clinic proceedings
2021

Ebstein's Anomaly: Review of Arrhythmia Types and Morphogenesis of the Anomaly.

JACC. Clinical electrophysiology
2021

Inadvertent irreversible closure of arterial duct following therapeutic use of transplacental indomethacin in a fetus with severe Ebstein's anomaly and circular shunt.

Ultrasound in obstetrics &amp; gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
2021

Impact of Cone vs. Hetzer Repair on Postoperative Outcomes in Patients With Ebstein's Anomaly: 10-Year Experience From a Single Institution.

Frontiers in cardiovascular medicine
2021

Clinical use of percutaneous mechanical circulatory assistance in a patient with end-stage right-sided heart failure and massive tricuspid insufficiency due to congenital heart disease: first-in-the-world case report.

European heart journal. Case reports
2022

Two decades of experience on ablation in children with Ebstein's anomaly.

Cardiology in the young
2021

A simplified repair method for adult Ebstein's anomaly.

Journal of cardiac surgery
2021

Surgical treatment of Ebstein anomaly in pediatric patients: A 10-year single-center study.

Journal of cardiac surgery
2021

Accessing the inaccessible: Stereotactic radioablation of premature ventricular complexes originating in the right ventricle in a patient with a mechanical tricuspid valve.

HeartRhythm case reports
2022

The Association of Age and Repair Modification with Outcome after Cone Repair for Ebstein's Malformation.

Seminars in thoracic and cardiovascular surgery
2021

COVID-19-Positive Patient and Hypoxemia: Are Lungs Always to Be Blamed?

JACC. Cardiovascular interventions
2021

Left Ventricular Pathology in Ebstein's Anomaly-Myocardium in Motion: CMR Insights Into Left Ventricular Fibrosis, Deformation, and Exercise Capacity.

Circulation. Cardiovascular imaging
2021

"Leafletization" of Atrialized Ventricular Septum Endocardium in Ebstein Anomaly.

The Annals of thoracic surgery
2021

Ebstein's anomaly in the neonate.

Indian journal of thoracic and cardiovascular surgery
2021

Hemodynamics and Clinical Implications of Occult Left Ventricular Dysfunction in Adults Undergoing Ebstein Anomaly Repair.

Circulation. Cardiovascular imaging
2022

From Safety to Benefit in Cell Delivery During Surgical Repair of Ebstein Anomaly: Initial Results.

The Annals of thoracic surgery
2020

Successful Radiofrequency Ablation of an Atrial Flutter in an Elderly Patient With Uncorrected Ebstein's Anomaly.

Cureus
2023

Commentary: Ventricular function improvement after the cone for Ebstein anomaly: It is time to incorporate magnetic resonance studies into every long-term postoperative protocol.

The Journal of thoracic and cardiovascular surgery
2020

Cone repair for Ebstein's anomaly and atrial fibrillation ablation in an adult patient.

Multimedia manual of cardiothoracic surgery : MMCTS
2021

Neonatal Cone Valvuloplasty for Pulmonary Atresia/Intact Ventricular Septum and Ebsteinoid Valve.

The Annals of thoracic surgery
2021

Electocardiographic features in Ebstein's disease.

La Tunisie medicale
2020

Patent foramen ovale and atrial septal defect.

Echocardiography (Mount Kisco, N.Y.)

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Doenças relacionadas

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Referências e fontes

Bases de dados externas citadas neste artigo

Publicações científicas

Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.

  1. Septal Leaflet Augmentation During the Da Silva Cone Repair: Valvar Function and Anatomical Features Compared to Non-Patch Repair.
    The Journal of thoracic and cardiovascular surgery· 2026· PMID 41819162mais citado
  2. Biventricular Repair in Symptomatic Neonates with Ebstein Anomaly: 25-30 years of follow-up.
    The Journal of thoracic and cardiovascular surgery· 2026· PMID 41780716mais citado
  3. Risk factors for morbidity and mortality in Ebstein's anomaly: a registry-based study of 398 patients.
    Clinical research in cardiology : official journal of the German Cardiac Society· 2026· PMID 41779126mais citado
  4. Changing Course-Starnes Takedown in High-Risk Children and Review of the Current Literature.
    Pediatric cardiology· 2026· PMID 41688615mais citado
  5. Use of right atrial wall to repair severely dysplastic tricuspid valve in an infant with Ebstein's anomaly.
    Multimedia manual of cardiothoracic surgery : MMCTS· 2026· PMID 41626808mais citado
  6. Left ventricular outflow tract obstruction after Ebstein tricuspid valve surgery: a case report.
    Int J Surg Case Rep· 2026· PMID 41938420recente
  7. Circular Shunt: A Loop Not to Be Ignored.
    J Cardiothorac Vasc Anesth· 2025· PMID 39706692recente
  8. Case report of Ebstein's anomaly in a young female.
    SAGE Open Med Case Rep· 2024· PMID 39588170recente
  9. Heterozygous nonsense variants in laminin subunit 3α resulting in Ebstein's anomaly.
    HGG Adv· 2023· PMID 37635785recente
  10. Impact of Cone vs. Hetzer Repair on Postoperative Outcomes in Patients With Ebstein's Anomaly: 10-Year Experience From a Single Institution.
    Front Cardiovasc Med· 2021· PMID 34422934recente

Bases de dados e fontes oficiais

Identificadores e referências canônicas usadas para montar este verbete.

  1. ORPHA:1880(Orphanet)
  2. OMIM OMIM:224700(OMIM)
  3. MONDO:0009144(MONDO)
  4. GARD:6313(GARD (NIH))
  5. Variantes catalogadas(ClinVar)
  6. Busca completa no PubMed(PubMed)
  7. Artigo Wikipedia(Wikipedia)
  8. Q277452(Wikidata)

Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.

Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar

Anomalia de Ebstein da válvula tricúspide
Compêndio · Raras BR

Anomalia de Ebstein da válvula tricúspide

ORPHA:1880 · MONDO:0009144
Prevalência
1-9 / 100 000
Herança
Autosomal dominant, Not applicable
CID-10
Q22.5 · Anomalia de Ebstein
CID-11
Início
All ages
Prevalência
1.25 (Europe)
MedGen
UMLS
C0013481
EuropePMC
Wikidata
Wikipedia
Papers 10a
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