Raras
Buscar doenças, sintomas, genes...
Óstio coronário, estenose ou atrofia
ORPHA:99087CID-10 · Q24.5CID-11 · LA86.YDOENÇA RARA

Esta é uma lista de prefixos, sufixos e radicais. A etimologia é uma ciência dedicada ao estudo das origens das palavras e das modificações sofridas por elas ao longo do tempo. Uma importante aplicação dos conhecimentos etimológicos é a compreensão de novos vocabulários.[carece de fontes?] Isso porque a língua portuguesa deriva de outros idiomas e se apropria de palavras estrangeiras, de modo que o significado de um termo poderia ser óbvio na língua original, mas deixou de o ser ao chegar aos falantes do português. Por meio da compreensão do que significavam, originalmente, prefixos, sufixos e radicais; podemos desmistificar o que indicam vocábulos do nosso cotidiano e, sobretudo, jargões técnicos, que resgatam muitos elementos do latim e do grego, por exemplo.

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Introdução

O que você precisa saber de cara

📋

Condição rara caracterizada pelo estreitamento (estenose) ou ausência (atresia) da abertura das artérias coronárias, comprometendo o fluxo sanguíneo para o músculo cardíaco. Pode levar a dor no peito, falta de ar e risco de infarto.

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SUS: Cobertura mínimaScore: 35%
Centros em: PA, PE, BA, CE, PB +10CID-10: Q24.5
🇧🇷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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Sinais e sintomas

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Últimos 10 anos200publicações
Pico2026199 papers
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2025Hoje · 2026
Publicações por ano (últimos 10 anos)

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Genética e causas

O que está alterado no DNA e como passa nas famílias

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Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

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Onde tratar no SUS

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

🇧🇷 Atendimento SUS — Óstio coronário, estenose ou atrofia

Centros de Referência SUS

24 centros habilitados pelo SUS para Óstio coronário, estenose ou atrofia

Centros para Óstio coronário, estenose ou atrofia

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.

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Publicações mais relevantes

Timeline de publicações
0 papers (10 anos)
#1

Fixel-Based Analysis of Pretreatment MRI Identifies White Matter Abnormalities in Pediatric Anti-NMDAR Encephalitis.

Journal of child neurology2026 Mar 25

Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is an autoimmune disorder in which conventional MRI often appears normal, leading to clinical-radiologic dissociation and hindering early diagnosis and monitoring. We retrospectively studied five pediatric patients with anti-NMDAR encephalitis and compared their pretreatment diffusion MRI to age- and sex-matched controls. Using fixel-based analysis (FBA), we quantified tract-specific white matter abnormalities at the individual level. All patients showed significantly reduced fiber density and cross-section, with patterns ranging from focal to widespread involvement. In two patients, FBA abnormalities corresponded to seizure lateralization on EEG despite normal MRI, emphasizing FBA's added value in detecting seizure-concordant injury. One patient, exhibiting the highest disease burden and marked CSF pleocytosis, demonstrated extensive white matter tract disruption. These findings indicate that FBA derived from pretreatment MRI can identify clinically significant white matter injury at disease onset in pediatric anti-NMDAR encephalitis. Future large-scale studies should explore its potential as an individualized biomarker, which may offer diagnostic and prognostic value beyond conventional imaging.

#2

Neuropsychological aspects of impulse control disorders in Parkinson's disease.

Frontiers in aging neuroscience2026

Impulse control disorders (ICDs), such as excessive gambling, compulsive sexual behavior, binge eating, compulsive shopping as well as punding, and the dopamine dysregulation syndrome, may arise as a debilitating neuropsychiatric complication in Parkinson's disease (PD). Although the pathophysiology is not fully understood, it likely involves mesolimbic dopaminergic overstimulation combined with disease-related vulnerabilities in reward, motivation, and inhibitory control networks. This narrative review summarizes evidence on the neuropsychological, affective, and behavioral traits associated with ICDs in PD, with a particular focus on epidemiology/clinical manifestations, neurobiological and pharmacological mechanisms, as well as prevention and management strategies. ICDs can affect up to 40% of PD patients and are strongly associated with dopamine agonist exposure, younger age of onset, premorbid personality traits, and neuropsychiatric comorbidities. Neuropsychological findings reveal abnormalities in several domains, including reflection impulsivity, temporal discounting, novelty seeking, risk processing, and inhibitory control, while mood disorders, sleep dysfunction, apathy, and anxiety further influence vulnerability and worsen behavioral dysregulation. Although general awareness for development of ICDs has been raised, they still represent a significant burden for patients and their family members and are a predictor of functional decline and lower quality of life. Management includes dopamine agonist withdrawal whenever possible, the cessation of fast acting dopaminergic agents and treatment of neuropsychiatric comorbidities. In selected cases, deep brain stimulation or continuous dopaminergic delivery should be considered, particularly in those experiencing persistent worsening of motor symptoms despite appropriate adjustment of dopaminergic medication.

#3

Role of Liver Biopsy in Biliary Atresia: Impact of Histological Fibrosis on Kasai Portoenterostomy Outcomes and Decision Making.

Pediatric gastroenterology, hepatology & nutrition2026 Mar

This study aimed to evaluate the effect of histological fibrosis on liver biopsy at presentation on the decision-making and outcomes of Kasai portoenterostomy (KPE), as well as the subsequent timing of liver transplantation. A retrospective, cross-sectional study of children <13 years old with biliary atresia (BA) seen at the Royal Hospital between January 2007 and December 2021. Forty children were diagnosed with BA, of whom 31 (77.5%) underwent a liver biopsy, and 26 (65.0%) underwent KPE. Thirty children (96.8%) had either complete or impending cirrhosis. Eleven children (42.3%) who underwent KPE received a liver transplantation at a median age of 26 months (interquartile range [IQR]=33-34). Four children did not undergo KPE, and seven (50.0%) of these underwent liver transplantation at a median age of 22 months (IQR=13-25). The age of liver transplantation did not differ statistically between the KPE group and the primary liver transplantation group (p=0.311). Three children (11.5%) were alive with their native liver following KPE at 5 years. The mortality rate was similar in the KPE and non-KPE groups (p=0.171). Of the 40 children with biliary atresia, 31 had a liver biopsy, with 30 (96.8%) exhibiting either complete or impending cirrhosis. Hepatic fibrosis did not impact the decision to perform KPE. The age of liver transplantation did not differ significantly between the KPE and non-KPE groups (median ages of 26 vs. 22 months, p=0.311).

#4

Comprehensive assessment of the genomic stability of human induced pluripotent stem cells for clinical applications.

Stem cell research &amp; therapy2026 Mar 25

Human induced pluripotent stem cells (hiPSCs) may acquire genomic alterations during reprogramming and culture, which poses significant risks for clinical applications. Current detection methods, such as karyotyping analysis, often fail to identify critical submicroscopic variations. This highlights an urgent need for comprehensive genomic surveillance strategies. Three human iPSC lines were continually cultured in vitro for 50 passages, with genome alterations evaluated every 10 passages. The evaluation methods included karyotyping to detect chromosomal abnormalities, optical genome mapping (OGM) to identify copy number variations (CNVs) and structural variants (SVs), whole-exome sequencing (WES) to detect coding mutations, and RNA sequencing (RNA-seq) to detect the changes of gene expression. We detected accumulating chromosomal abnormalities (e.g., trisomy 12), SVs, CNVs, and sequence mutations in three hiPSC lines during extended culture. OGM effectively identified SVs and CNVs below karyotyping resolution, particularly recurrent genome abnormalities such as gains on chr17q, chr12p and chr20q. WES revealed coding mutations, including germline short variants and newly acquired somatic mutations, some of which were associated with tumors or diseases, such as CDH1, BCOR. Transcriptional changes correlated with genomic alterations, including dysregulation of oncogenes such as BCL2L1, KRAS and MDM2. Results demonstrate that each method had unique detection capabilities and limitations, and only integrative approaches can comprehensively identify genomic abnormalities. This study established a comprehensive strategy for evaluating the genomic alterations of hiPSCs by integrating karyotyping, OGM, WES, and RNA-seq. This comprehensive strategy can be applied to scenarios such as hiPSC clone screening, establishment of cell bank passages, and quality control of hiPSC-derived products. It provides a reliable genetic stability evaluation protocol to support the safe clinical application of hiPSC-related products.

#5

The diagnostic value of ultrasound viscoelastic imaging for biliary and vascular complications after liver transplantation: a single-center retrospective study.

BMC gastroenterology2026 Mar 24

Postoperative biliary and vascular complications (including stenosis, thrombosis, and occlusion) after liver transplantation (LT) can impair graft function, increase reoperation needs, and elevate patient mortality, significantly affecting long-term survival. The clinical reference standards magnetic resonance cholangiopancreatography (MRCP) for biliary complications is expensive and time-consuming, while computed tomography angiography (CTA) for vascular complication involves ionizing radiation and allergic reaction to contrast agents, limiting their repeated use during follow-up. Ultrasound viscoelastic imaging (UVI), an affordable, non-invasive technique, could be an effective alternative. This study aims to assess the clinical value of UVI in auxiliary diagnosis of biliary and vascular complications post-LT. Between June 2024 and August 2025, 141 LT patients who underwent UVI were retrospectively analyzed, including 25 with repeated examinations (intervals of 1-4 weeks). UVI parameters included Young's modulus, viscosity, and dispersion coefficients. MRCP and CTA served as reference standards for biliary and vascular complications, respectively. Statistical analysis was performed using SPSS 27.0 (P < 0.05). Independent t-tests or non-parametric tests were applied, and generalized estimating equations (GEE) was used for patients with multiple UVI measurements. Among 116 patients with a single UVI, mean Young's modulus, viscosity, and dispersion values were 12.30 ± 6.41 kPa, 2.3 ± 0.9 Pa·s, and 5.25 ± 1.81 m/s/kHz, respectively. Patients with biliary complications (n = 52) showed significantly higher viscoelastic values than those without (n = 64). In vascular complications (n = 10), only minimum viscosity differed significantly from controls. In patients with repeated UVI, GEE analysis revealed significant temporal changes in elasticity, viscosity, and dispersion parameters after liver transplantation (all P < 0.001). Significant time-complication interactions were identified for biliary complications and for most vascular parameters, suggesting distinct longitudinal patterns between patients with and without complications. Viscoelasticity values increased in the presence of biliary and vascular complications, likely due to hemodynamic abnormalities and tissue inflammation. These findings suggest that UVI can be a valuable tool for monitoring biliary and vascular complications after LT, providing non-invasive, reliable, and repeated assessments of graft health.

Publicações recentes

Ver todas no PubMed

📚 EuropePMCmostrando 200

2026

Rapidly Progressive Kidney Failure With Transient Non-Cystic Kidney Enlargement: A Case Report Highlighting Delayed Medullary Cyst Formation.

Nephrology (Carlton, Vic.)
2026

Fixel-Based Analysis of Pretreatment MRI Identifies White Matter Abnormalities in Pediatric Anti-NMDAR Encephalitis.

Journal of child neurology
2026

[Optimisation of psychopharmacological treatment strategies by using therapeutic drug monitoring].

Therapeutische Umschau. Revue therapeutique
2026

Leprosy in Pregnancy: A Systematic Review of Maternal Characteristics, Complications, and Neonatal Outcomes.

International journal of women's health
2026

Machine Learning-Based Diagnostic Models for Early Gastric Cancer Using Clinical Laboratory Indicators.

International journal of general medicine
2026

SARS-CoV-2 spike S1-mediated HIF-2α activation in retinal endothelial cells suggests a mechanism contributing to post-COVID endothelial dysfunction.

Frontiers in immunology
2026

Severe Fetal Anaemia Secondary to Fetomaternal Haemorrhage: A Case Report Exploring Aetiologies and Diagnostics.

Cureus
2026

Neuropsychological aspects of impulse control disorders in Parkinson's disease.

Frontiers in aging neuroscience
2026

Difference in Respiratory Function Between GOLD Stage 1 and Preserved Ratio Impaired Spirometry as Assessed by Impulse Oscillometry and Spirometry.

International journal of chronic obstructive pulmonary disease
2026

A Case of Solar Maculopathy Secondary to Reflected Sunlight During Garden Tiling.

Cureus
2026

Bilateral Optic Disc Edema Secondary to Severe Vitamin A Deficiency: A Rare Cause of Acute Vision Loss.

Case reports in ophthalmology
2026

Prenatally Diagnosed Proximal Femoral Focal Deficiency: A Report of Two Cases.

International medical case reports journal
2026

Calcified frontal neurocysticercosis presenting with acute psychosis in a non-endemic context: a case report.

Frontiers in psychiatry
2026

Role of Liver Biopsy in Biliary Atresia: Impact of Histological Fibrosis on Kasai Portoenterostomy Outcomes and Decision Making.

Pediatric gastroenterology, hepatology &amp; nutrition
2026

Utility of Novel Lipid Parameters for Risk Stratification in Patients with Diabetes and STEMI-from a Prospective Study.

Vascular health and risk management
2026

Predicting adverse outcomes after cardiac surgery and structural interventions: the role of right ventricular function.

Future cardiology
2026

A Case of Restrictive Dermopathy With Atypical Cardiac Anomalies and a Novel ZMPSTE24 Variant.

American journal of medical genetics. Part A
2026

Metabolic syndrome and serum uric acid level in children and adolescents with hypertension.

Journal of hypertension
2026

Comprehensive assessment of the genomic stability of human induced pluripotent stem cells for clinical applications.

Stem cell research &amp; therapy
2026

A novel MMP13 frameshift variant causes short stature via enhanced MMP13-HSPA5 interaction and activated endoplasmic reticulum stress.

Clinical and translational medicine
2026

The diagnostic value of ultrasound viscoelastic imaging for biliary and vascular complications after liver transplantation: a single-center retrospective study.

BMC gastroenterology
2026

Identification of common genetic and molecular signatures in migraine and comorbid conditions.

The journal of headache and pain
2026

Valproic acid for the management of agitation in neurosurgical intensive care unit patients.

Neurocritical care
2026

EBV-associated histological transformation of marginal zone lymphomas: two case reports and a literature review.

Virchows Archiv : an international journal of pathology
2026

Monitoring the Progression of Pre-Ataxic Gait in SCA2 with Inertial Sensors Over Four Years.

Cerebellum (London, England)
2026

Different effect of aldosterone on corrected HCO3- across primary aldosteronism subtypes.

Hypertension research : official journal of the Japanese Society of Hypertension
2026

Predictive value of high-density lipoprotein cholesterol and the cardio-ankle vascular index on cardiovascular outcomes in subjects with cardiovascular risks: the COUPLING Study.

Hypertension research : official journal of the Japanese Society of Hypertension
2026

IGFBP3 repression driven by inflammation links air pollution to placental and developmental defects.

EMBO molecular medicine
2026

Integrated transcriptomics and proteomics analysis reveal potential target in pediatric primary restrictive cardiomyopathy.

Pediatric research
2026

Exploratory characterization of gut microbiota and cognitive profiles in adolescents with subthreshold depression: a shotgun metagenomics sequencing study.

Npj mental health research
2026

Deep learning-based quantitative CT assessment of interstitial lung abnormalities: prognostic risk thresholds in a health screening population.

Scientific reports
2026

EXPRESS: Feline plasma cell pododermatitis with concurrent glomerular disease: a case series of 25 cats.

Journal of feline medicine and surgery
2026

Accelerated 3D MRI for ARIA monitoring in Alzheimer's disease.

Alzheimer's &amp; dementia : the journal of the Alzheimer's Association
2026

Dyslipidemia and therapies after heart transplantation: Current evidence and future directions.

Journal of clinical lipidology
2026

Bedside contrast-enhanced ultrasound: Clinical applications for internal medicine.

European journal of internal medicine
2026

A new system for custom helical mandibular distraction: a bench study on anatomical models.

International journal of oral and maxillofacial surgery
2026

[Research progress on the involvement of glucose transporter-mediated cerebral glucose metabolism in the regulation of sepsis-associated encephalopathy].

Zhonghua wei zhong bing ji jiu yi xue
2026

[Related factors and characteristics of common disease multimorbidity among primary and secondary school students in Hunan Province].

Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi
2026

Effects of ACE inhibitor and afterload reduction in single ventricles following bidirectional Glenn.

Open heart
2026

Diagnostic Clues and Pitfalls in Pontocerebellar Hypoplasia Type 2A.

Pediatric neurology
2026

Glucose abnormalities in infants with birth asphyxia are associated with later neurological diagnoses.

Early human development
2026

Molecular mechanisms and treatment strategies for bone defects: From hypoxia-inflammation-ferritinophagy vicious cycle to intelligent biomaterial application.

Tissue &amp; cell
2026

Ferritin-positive microglial clusters associate with microvessels and markers of vascular injury in MCI and Alzheimer's disease.

Neurobiology of aging
2026

Reconstruction of an unguarded tricuspid orifice using a simplified sliding plasty technique.

Interdisciplinary cardiovascular and thoracic surgery
2026

Design and Optimization of Lysosome-Targeted β-Galactoside Senolytic Prodrugs: Harnessing the Aromatic Ring of Self-Immolative Linkers.

Journal of medicinal chemistry
2026

Biologically grounded on-chip model identifies selective topographic reorganization within hyperexcitable corticostriatal networks.

Proceedings of the National Academy of Sciences of the United States of America
2026

Congenital Corneal Staphyloma in an Asian Infant With Kabuki Syndrome Confirmed by a KMT2D Mutation.

The Journal of craniofacial surgery
2026

Bert W. O'Malley (1936-2025): A great scientist, mentor, and proud Irishman.

Proceedings of the National Academy of Sciences of the United States of America
2026

Widespread structural and functional brain alterations in COVID-19: a systematic review of MRI studies.

Cerebral cortex (New York, N.Y. : 1991)
2026

Diffusion tensor imaging with 3D high-resolution MRI of lumbosacral nerve roots in lumbar disc herniation with radiculopathy and its clinical correlations: a prospective study.

La Radiologia medica
2026

Development of a Bedside Scoring Tool to Screen for Biliary Atresia in Infants with Neonatal and Infantile Cholestasis in a Resource-limited Setting: an Observational Study.

Indian pediatrics
2026

Perivascular fluid clearance links choroid plexus changes to cognitive performance in cerebral small vessel disease.

Brain informatics
2026

Combined prognostic impact of complex karyotype and KIT mutations refines risk stratification in t(8;21) acute myeloid leukemia.

Cancer
2026

Imaging-based anatomical study of torus mandibularis: morphological features identified by computed tomography and their correlation with panoramic radiographic appearances.

Oral radiology
2026

Diagnostic performance of triplanar real-time chest magnetic resonance imaging in preschool children - comparison with dedicated lung magnetic resonance imaging.

Pediatric radiology
2026

Assessing the feasibility of neonatal chest MRI for bronchopulmonary dysplasia using a standard 1.5-Tesla scanner.

European radiology
2026

The diagnostic value of magnetic resonance defecography in differentiating evacuation disorders among patients with manometric dyssynergia.

Abdominal radiology (New York)
2026

VF Arrest at Rest in a Teenager With Anomalous Origin of Coronaries and DSG2 Variant.

JACC. Case reports
2026

Clinical characteristics and surgical outcomes of Rasmussen encephalitis: A retrospective dual-center cohort study.

Epilepsia
2026

Trifurcation of the sciatic nerve. Short bifurcation of the common fibular nerve in the high gluteal region: a case study.

Folia morphologica
2026

Research Hotspots and Trends in Ciliopathies: A Bibliometric and Visualization Analysis.

BioMed research international
2026

Paraneoplastic Hepatitis Associated with Relapsed Nodular Lymphocyte-Predominant Hodgkin Lymphoma.

Hematology reports
2026

Cochlear Implantation in Down Syndrome: Functional Outcomes, Challenges, and Management Strategies.

Audiology research
2026

Differentiating Atypical BPPV from Central Positional Vertigo: A Narrative Review.

NeuroSci
2026

Finding the Genetic Diagnosis for a Mother and Daughter With a Novel Phenotype of Hand and Foot Abnormalities and Severe Pectus Excavatum Previously Reported in Am J Med Genet Part A by Low K et al. (2013).

American journal of medical genetics. Part A
2026

The interaction between NPMc+ and Orai1 induces abnormal calcium influx to facilitate leukemogenesis.

The FEBS journal
2026

Hemodynamic Mechanisms in Venous Pulsatile Tinnitus: A 4D Flow MRI Analysis of Transverse-Sigmoid Sinus Abnormalities.

Journal of magnetic resonance imaging : JMRI
2026

Clinical and genetic basis of congenital gonadotropin deficiency.

Human reproduction open
2026

Gastric Bypass Presenting as Mixed Beriberi and Wernicke Encephalopathy.

Cureus
2026

Effect of Lee Silverman Voice Treatment-BIG Intervention Versus Balance Training via Tele-rehabilitation on Balance and Functional Mobility Among Community-Dwelling Elderly: A Comparative Study.

Cureus
2026

Incomplete Kawasaki Disease Presenting With Coronary Artery Aneurysms in a 2.5-Month-Old Infant: A Case Report.

Cureus
2026

Vestibular functioning in people with Parkinson's disease.

International journal of audiology
2026

Distinct brain volume abnormalities in clinical high-risk individuals: pre- and post-antipsychotic treatment.

Psychological medicine
2026

The Selection of an Interposition Graft for Portal Vein Reconstruction: Maximizing the Availability of Autologous Vessels.

Pediatric transplantation
2026

Labyrinthine Abnormalities on MRI in Untreated Otosclerosis: Prevalence and Clinical Relevance.

The Laryngoscope
2026

Predictors of chronic kidney diseases and kidney failure in patients with CAKUT: a cohort study.

International urology and nephrology
2026

Comparative evaluation of multimodal large language models for diagnostic accuracy in pediatric electrocardiography: a prospective comparative diagnostic accuracy study.

European journal of pediatrics
2026

Development of metabolic syndrome by increasingly fructose-enriched water in Wistar rats.

Journal of molecular histology
2026

Semaglutide restores metabolic and structural homeostasis along the gut-heart-metabolic axis in a cafeteria diet-induced obesity model.

Scientific reports
2026

A hybrid pipeline for carotid artery segmentation using YOLOv11n and contour models.

Scientific reports
2026

Loss of DIAPH3 accelerates glioma genesis in mice.

Cell death &amp; disease
2026

HNRNPH1 drives glioblastoma progression by regulating the splicing of cell cycle genes.

Cell death &amp; disease
2026

The amino acid transporter LAT1 coordinates proper motor function at the perinatal stage.

Cell death &amp; disease
2026

X-linked adrenoleukodystrophy as an etiological cause of progressive spastic paraplegia: A case report.

The Journal of international medical research
2026

ASPH-related ectopia lentis revisited: genetic variability, clinical diversity, and evolving therapeutic approaches.

Ophthalmic genetics
2026

Lingual haemangiosarcoma in a French Bulldog: atypical clinical presentation.

Australian veterinary journal
2026

Clinical Diversity in Currarino Syndrome: Insights From Monozygotic Twins and a Single-Center Retrospective Study.

Congenital anomalies
2026

Revisiting Fundoplication in Esophageal Atresia: Implications for Nutrition, Stricture Management, and Wrap Type.

Journal of pediatric surgery
2026

VACTERL Association in Screened Patients with Esophageal Atresia: A Retrospective Cohort Study.

Journal of pediatric surgery
2026

Artificial Intelligence Applications in COVID-19-Associated Coagulopathy: Lessons Learned.

Seminars in thrombosis and hemostasis
2026

Chronic nonbacterial osteomyelitis: current perspectives in pediatric practice.

The Turkish journal of pediatrics
2026

Non-ketotic hyperglycaemic hemichorea as the first manifestation of undiagnosed diabetes mellitus in an elderly patient.

Endocrinology, diabetes &amp; metabolism case reports
2026

Abnormality detection in soft tissues: Multivariate outlier framework based on multi mechanical characterization using indentation.

Medical engineering &amp; physics
2026

Age, sex, smoking-specific prevalence and progression in interstitial lung abnormality: patient-level meta-analysis.

Annals of the American Thoracic Society
2026

Dynamic Cytogenetic Evolution in Multiple Myeloma: Prognostic Implications from Diagnosis to First Relapse.

The oncologist
2026

Perineural spread of colorectal carcinoma into the sciatic nerve with positive circulating tumor DNA test: illustrative case.

Journal of neurosurgery. Case lessons
2026

Time lag between functional and structural lymphatic changes after lymphadenectomy: Insights from ICG lymphography and lymphatic ultrasound.

PloS one
2026

Efficacy of Lithium Carbonate Combined with Olanzapine, Risperidone, or Quetiapine in Bipolar Disorder Treatment and Effects on Glycolipid Metabolism.

Journal of visualized experiments : JoVE
2026

N6-methyladenosine-modified miR-873 promotes receptor-interacting protein kinase 3-mediated necroptosis after intracerebral hemorrhage in mice and HT22 cells.

Neuroreport
2026

Environmental and Lifestyle Exposures and Male Factor Subfertility Proportion Among Infertile Couples: A Clinic-Based Multicenter Cross-Sectional Analysis from Indian Male Factor Subfertility Evaluation (IM-FaST) Study.

Environmental science and pollution research international
2026

OPM-based fetal magnetocardiography: fetal cardiac time intervals in healthy pregnancies compared to postnatal ECGs.

Archives of gynecology and obstetrics
2026

Navigating the spectrum: a comprehensive approach to fetal lung abnormalities in ultrasound and magnetic resonance imaging.

Pediatric radiology
2026

Update on Cerebral/Cortical Visual Impairment (CVI) in Children.

International ophthalmology clinics
2026

Congenital Optic Nerve Anomalies and Associated Systemic Conditions.

International ophthalmology clinics
2026

Tailored Charles' Procedure and Vascularized Lymph Node Transfer for Advanced Stage Klippel-Trenaunay Syndrome.

Acta chirurgica Belgica
2026

Vestibular dysfunction and infratentorial MRI abnormalities in multiple sclerosis.

Irish medical journal
2026

The endocrine impact of immunotherapy: audit and future service implications.

Irish medical journal
2026

Ovarian Hormones Moderate Systolic Hypertension in Female Eln Haploinsufficient Mice.

American journal of physiology. Renal physiology
2026

A Triboelectric Nanogenerator-Based Electromechanical Synchronized Sensing Probe for Simultaneous Detection of Cardiac Physiological Activities.

ACS sensors
2026

First Generation Proteolysis Targeting Chimeras (PROTACs) for the Treatment of Progeria.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)
2026

REM Sleep Abnormalities in Children With Autism Spectrum Disorder.

Autism research : official journal of the International Society for Autism Research
2026

Case Report: Successful natural conception and delivery in a primary cancer survivor involving the reproductive, respiratory, and endocrine systems auth.

Frontiers in oncology
2026

Associations of triglyceride-glucose-body mass Index and C-reactive protein with isolated nocturnal hypertension: evidence from a retrospective observational study.

Frontiers in cardiovascular medicine
2026

Impact on mitral regurgitation in patients with AVB undergoing permanent pacemaker implantation: left bundle branch pacing vs. right ventricular septum pacing.

Frontiers in cardiovascular medicine
2026

Association between plaque characteristics and side-branch compromise in left main bifurcation lesions after a single-stent crossover technique: insights from an optical coherence tomography study.

Frontiers in cardiovascular medicine
2026

A Survey on the Treatment of Extra-Articular Malunions of the Distal Radius.

Journal of wrist surgery
2026

Peripheral Nerve Ultrasound Findings in Leprosy: A Scoping Review of Echogenicity, Cross-Sectional Area, and Vascularization Across 15 Studies.

Clinical, cosmetic and investigational dermatology
2026

Insights on Acute and Chronic Lacquer Cracks as Imaged with Visible Light OCT.

Ophthalmology science
2026

Unexpected detection of clear cell sarcoma of soft tissue during single-channel endoscopic carpal tunnel release for recurrent carpal tunnel syndrome: a case report with literature review.

Frontiers in surgery
2026

The clinical, serological and myopathological features of a cohort of Chinese patients with inclusion body myositis: a single center analysis.

Frontiers in immunology
2026

Ischemic Stroke as the Initial Presentation of Advanced Pancreatic Adenocarcinoma: A Case of Marantic Endocarditis.

Cureus
2026

Gastric Mucosal Biopsy Revealing Immunoglobulin G4 (IgG4)-Related Disease With Subtle Macroscopic Changes: A Case Report.

Cureus
2026

Brown Tumor in a Patient With End-Stage Renal Disease: A Case Report of Secondary Hyperparathyroidism Complications.

Cureus
2026

Novel Compound Heterozygous CFAP53 Variants in a Fetus With Situs Inversus Totalis: A Case Report.

Cureus
2026

The Hidden Face of Lyme Disease: Neuroinfection With Cranial Nerve Involvement.

Cureus
2026

Fetal echocardiography combined with serum biomarkers for early diagnosis of congenital heart disease and birth defect risk prediction.

American journal of translational research
2026

Trousseau's syndrome with cerebral infarction as the first manifestation.

American journal of translational research
2026

Diagnosis of malignant pleural effusion using thoracoscopy combined with confocal endomicroscopy: a case report.

American journal of translational research
2026

Altered EEG microstate associated with anxiety and somatization symptoms in major depressive disorder.

Frontiers in psychiatry
2026

An exploratory study of altered regional homogeneity in Parkinson's disease with depression.

Frontiers in psychiatry
2026

Pressure cycling technology-assisted data-independent acquisition proteomics reveals molecular alterations and potential therapeutic targets in minor glomerular abnormalities.

Precision clinical medicine
2026

Marked clinical and haemodynamic improvement with sotatercept in severe refractory pulmonary arterial hypertension associated with corrected complex congenital heart disease.

Respiratory medicine case reports
2026

Clinical characteristics and long-term treatment outcomes of patients with new-onset epileptic seizures associated with COVID-19 infection.

Frontiers in neurology
2026

Postoperative acute ultra-early fish mouthing of a Surpass Evolve flow diverter leading to ischemic complication.

Radiology case reports
2026

Incidental Detection of Glutamate Formiminotransferase Deficiency Through Newborn Screening in a Clinically Asymptomatic Infant: Molecular Findings and Counseling Considerations.

Cureus
2026

Interconnected roles of astrocytes and the blood-brain barrier in Parkinson's disease: pathological evidence, mechanistic insights, and knowledge gaps.

Frontiers in aging neuroscience
2026

Diagnostic odyssey of a German shepherd dog with disseminated Penicillium labradoris infection: a case report.

Frontiers in veterinary science
2026

Complex interactions of gut-derived short-chain fatty acids in hyperuricemia and gout pathophysiology.

Frontiers in microbiology
2026

Case Report: Genetic testing reveals Wilson disease with familial hypertriglyceridemia in a 12-year-old boy.

Frontiers in pediatrics
2026

Case Report: Pediatric chylous ascites beyond congenital malformations-infectious causes and nutritional management with a literature review.

Frontiers in pediatrics
2026

APOE3 astrocytes can rescue lipid abnormalities and dystrophic neurites of APOE4 human neurons.

PNAS nexus
2026

Metabolic pathways and chemotherapy resistance in acute myeloid leukemia (AML): Insights into Enoyl-CoA hydratase domain-containing protein 3 (ECHDC3) as a potential therapeutic target.

Cancer pathogenesis and therapy
2026

Early Binding of Anti-Amyloid Antibodies to CAA Drives Complement Activation, Inflammation and ARIA in Mice.

bioRxiv : the preprint server for biology
2026

Preclinical validation of AAV9-TECPR2 gene therapy in a novel knock-in model of TECPR2-related disorder.

bioRxiv : the preprint server for biology
2026

Association of Ambulatory Arterial Pressure Index with Circadian Blood Pressure Patterns in Patients with Primary Hypertension and Coronary Artery Disease.

International journal of general medicine
2026

TEM-based Study of the Phenotype of Astrocytes Differentiated from Induced Pluripotent Stem Cells from a Healthy Donor and a Patient with Parkinson's Disease.

Sovremennye tekhnologii v meditsine
2026

Managing metabolic risks in coronary artery disease: A scoping review of recent clinical and therapeutic evidence.

Journal of diabetes and metabolic disorders
2025

Molecular insights into foveal hypoplasia: development, genetics, mechanisms, and models.

Molecular vision
2026

Case Report: Maculopathy following standard dose intracameral cefuroxime injection during ICL surgery.

Frontiers in ophthalmology
2026

Overcoming Complexity: Percutaneous Embolization for Hepatic Artery Pseudoaneurysms in Hereditary Hemorrhagic Telangiectasia (HHT).

The Indian journal of radiology &amp; imaging
2026

Novel PCDH12 pathogenic missense variants cause neurodevelopmental disorders with ocular malformation.

medRxiv : the preprint server for health sciences
2026

Automated machine learning of echocardiographic strain enables identification of early myocardial changes in pre-symptomatic TTR carriers.

medRxiv : the preprint server for health sciences
2026

Adult Life Course Trajectories of Lung Function and the Development of Interstitial Lung Abnormalities: The CARDIA Lung Study.

medRxiv : the preprint server for health sciences
2026

Stricture classification of pediatric esophageal strictures (SCOPES): A novel tool to predict response to endoscopic therapy.

Journal of pediatric gastroenterology and nutrition
2026

Hyperactive GNAQ in endothelial cells causes blood vessel malformation in developing mouse skin.

Development (Cambridge, England)
2026

Recovery trajectories of TAFRO syndrome: a single-center case series highlighting prolonged thrombocytopenia and anasarca.

Immunological medicine
2026

Comparison of Oral Cephalosporin and Penicillin Step-Down Therapy for the Treatment of Gram-Negative Blood Stream Infections: A Retrospective Observational Study.

The Annals of pharmacotherapy
2026

Reporting a Novel Disease Causing Variant in PGAP3 Associated With Hyperphosphatasia and Intellectual Disability: A Case Report and Comprehensive Literature Review.

Molecular genetics &amp; genomic medicine
2026

TENT-5 polyadenylates and regulates male-specific transcripts in Caenorhabditis elegans.

G3 (Bethesda, Md.)
2026

Human blood vessel organoids recapitulate key mechanisms of transition from vasculopathy to fibrosis in systemic sclerosis.

Annals of the rheumatic diseases
2026

[A case of left ventricular apical hypoplasia].

Zhonghua xin xue guan bing za zhi
2026

Allele-specific effects of distinct SLC26A4 variants on cochlear function and transcriptomic programs in compound heterozygous models.

Bioscience trends
2026

Proteomic and Phenotypic Profiling of Replicative-Senescent HFF-1 Fibroblasts Under Brief Heat Shock.

Cell stress &amp; chaperones
2026

PRAMEL12 orchestrates spermiogenesis to ensure male fertility in mice.

The Journal of biological chemistry
2026

Hippocampal subfields volumes as biomarkers for early diagnosis of asymptomatic manganese overexposure.

NeuroImage
2026

Aberrant structural-functional connectivity coupling in migraineurs is associated with mental behavioral scores and neurotransmitter.

Progress in neuro-psychopharmacology &amp; biological psychiatry
2026

Age-Dependent Decline in Plasmalogen Biosynthesis Impairs Stress-Induced Mitochondrial Fission in Drosophila.

Experimental cell research
2026

INCIDENCE and risk factors associated with fetal heart rate abnormalities within one hour of labor epidural analgesia initiation: a retrospective cohort study.

Journal of gynecology obstetrics and human reproduction
2026

Ring Chromosome 6: A Case Report and Literature Review.

Journal of gynecology obstetrics and human reproduction
2026

miR-7480-5p/SIRT3/GSH axis mediates selenium Deficiency-Exacerbated trimethyltin chloride-induced ferroptosis in chicken thymus.

Journal of advanced research
2026

Evaluation of Lung Disease in Adults with Osteogenesis Imperfecta: A Cross-Sectional, Multi-Center Study.

Chest
2026

Myo-inositol elevation as an in vivo marker of reactive gliosis in pediatric Friedreich ataxia: evidence from HERMES-edited MR spectroscopy.

NeuroImage. Clinical
2026

Glutaminase deficiency provides insight to the role of glutamine accumulation and neurotoxicity.

Molecular genetics and metabolism
2026

Preimplantation genetic testing for meiotic aneuploidy in trophectoderm biopsies - is it time to change our approach?

Reproductive biomedicine online
2026

"It's a journey": Psychosocial perspectives on parenting a young child with esophageal atresia.

Pediatric surgery international
2026

A national database study of adjuvant steroids following Kasai portoenterostomy for biliary atresia.

Pediatric surgery international
2026

Pulmonary Function in Pediatric Inflammatory Bowel Disease: A Systematic Review and Meta-Analysis.

Pediatric pulmonology
2026

Sustainable NADES and Ultrasound-Assisted Extraction of PFAS and Microplastics in Environmental Matrices.

Critical reviews in analytical chemistry
2026

Giant parieto-occipital encephaloceles: always a dismal prognosis? A case report and review of the literature.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
2026

Circulating cardiometabolic metabolite profiles associated with ambient air pollution and atrial fibrillation risk: a prospective cohort study.

Cardiovascular diabetology
2026

Nanomaterials for Alzheimer's disease: emerging strategies in diagnosis and therapy.

Journal of nanobiotechnology
2026

Laparoscopic management of congenital pyloric Atresia: A case series and surgical perspective.

Pediatrics and neonatology
2026

Definition, diagnosis, treatment for scleroderma primary heart involvement.

Best practice &amp; research. Clinical rheumatology
2026

Resveratrol Protects Lens Epithelial Cells and Delays Cataract Development via Inhibiting TXNIP Mediated Oxidative Stress and Apoptosis.

Experimental eye research
2026

Peroxisomal dynamics in Degenerative retinopathies: implications of retinal lipid metabolism and therapeutic potential.

Experimental eye research
2026

Prenatal and Postnatal Choline Supplementation Alters Metabolic Dysfunction-Associated Steatohepatitis (MASH) Phenotypes in Offspring Exposed to Maternal Obesity and Following a Western Diet into Adulthood: a Preliminary Study.

The Journal of nutritional biochemistry
2026

KCNH2 Duplication Variant (c.2164_2181dup) Associated with Sudden Cardiac Death in a Family with Congenital Long QT Syndrome.

The Canadian journal of cardiology
2026

Dynamic characteristics of brain networks in patients with obsessive-compulsive disorder based on naturalistic paradigm.

Journal of affective disorders
2026

The pathogenic ADAMTSL2 D167N variant causes geleophysic dysplasia-like connective tissue changes in mice.

The American journal of pathology
2026

Imprinting disorders and multiple imprinting abnormalities (multilocus imprinting disturbances): new diagnoses, new perspectives.

Annales d'endocrinologie
2026

Severe Varicella-Zoster Virus Encephalitis with Extreme Cerebrospinal Fluid Protein Elevation and Delayed Hydrocephalus in an Immunocompetent Patient in Shanghai.

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
2026

Rheumatic Heart Disease Is Not Over: Cardiac Cirrhosis and Multivalvular Sequelae in an Endemic Setting - A Case Series and Review.

Current problems in cardiology
2026

Combined toxicity of triclocarban and bisphenol S in zebrafish: Multi-level synergistic effects and driving mechanisms.

Journal of hazardous materials
2026

Genomic profiling of meiotic errors and early malignant transformation events in ovarian mature teratoma.

Reproduction (Cambridge, England)
2026

Prevalence and Risk of Falls and Fractures in the Idiopathic Inflammatory Myopathies: A Cross-Sectional Study of 470 Patients.

Rheumatology and therapy
2026

Hypocoagulability among people living with HIV at Hoima Regional Referral Hospital, Western Uganda: a cross-sectional study.

HIV research &amp; clinical practice
2026

Riluzole Restores Circuit and Behavioral Function Altered by Allele-Specific Expression-Mediated LINC02449-CPLX1 Dysregulation.

Schizophrenia bulletin
2026

An Efficient Contrastive Deep Learning Model for Identifying Schizophrenia-Specific Neuroanatomical Variations.

Schizophrenia bulletin
2026

Short-, Medium-, and Long-Term Cardiometabolic Outcomes in First-Episode Psychosis: A Systematic Review and Meta-analysis.

Schizophrenia bulletin
2026

Robo2-Nrxn3 Deficiency: A Molecular Hub Linking Excitation-Inhibition Imbalance to the Pathogenesis of Schizophrenia.

Schizophrenia bulletin

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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. Fixel-Based Analysis of Pretreatment MRI Identifies White Matter Abnormalities in Pediatric Anti-NMDAR Encephalitis.
    Journal of child neurology· 2026· PMID 41878763mais citado
  2. Neuropsychological aspects of impulse control disorders in Parkinson's disease.
    Frontiers in aging neuroscience· 2026· PMID 41878312mais citado
  3. Role of Liver Biopsy in Biliary Atresia: Impact of Histological Fibrosis on Kasai Portoenterostomy Outcomes and Decision Making.
    Pediatric gastroenterology, hepatology &amp; nutrition· 2026· PMID 41877709mais citado
  4. Comprehensive assessment of the genomic stability of human induced pluripotent stem cells for clinical applications.
    Stem cell research &amp; therapy· 2026· PMID 41877289mais citado
  5. The diagnostic value of ultrasound viscoelastic imaging for biliary and vascular complications after liver transplantation: a single-center retrospective study.
    BMC gastroenterology· 2026· PMID 41877027mais citado
  6. Association between plaque characteristics and side-branch compromise in left main bifurcation lesions after a single-stent crossover technique: insights from an optical coherence tomography study.
    Front Cardiovasc Med· 2026· PMID 41869527recente
  7. Coronary artery anomalies in common arterial trunk: proposal of a new anatomical classification.
    Interdiscip Cardiovasc Thorac Surg· 2026· PMID 41863318recente
  8. Concomitant Discovery and Treatment of Acquired and Congenital Cardiac Disease.
    JACC Case Rep· 2026· PMID 41847778recente
  9. Dynamic Flap at the Coronary Opening Mimicking Left Main Disease: A Rare Coronary Obstruction Cause.
    JACC Case Rep· 2026· PMID 41774031recente
  10. All three coronary arteries and a separate conus branch arising from the right sinus of Valsalva in an octogenarian with an acute myocardial infarction: a case report.
    Eur Heart J Case Rep· 2026· PMID 41757253recente

Bases de dados e fontes oficiais

Identificadores e referências canônicas usadas para montar este verbete.

  1. ORPHA:99087(Orphanet)
  2. MONDO:0020423(MONDO)
  3. GARD:19643(GARD (NIH))
  4. Busca completa no PubMed(PubMed)
  5. Q55789356(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

Compêndio · Raras BR

Óstio coronário, estenose ou atrofia

ORPHA:99087 · MONDO:0020423
CID-10
Q24.5 · Malformações dos vasos coronários
CID-11
MedGen
UMLS
C5575847
Wikidata
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