Um problema nas artérias do coração que se caracteriza por uma origem, um trajeto ou uma estrutura diferente do normal em uma ou mais dessas artérias, presente desde o nascimento.
Introdução
O que você precisa saber de cara
Um problema nas artérias do coração que se caracteriza por uma origem, um trajeto ou uma estrutura diferente do normal em uma ou mais dessas artérias, presente desde o nascimento.
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Entender a doença
Do básico ao detalhe, leia no seu ritmo
Preparando trilha educativa...
Sinais e sintomas
O que aparece no corpo e com que frequência cada sintoma acontece
Partes do corpo afetadas
+ 12 sintomas em outras categorias
Características mais comuns
Os sintomas variam de pessoa para pessoa. Abaixo estão as 27 características clínicas mais associadas, ordenadas por frequência.
Linha do tempo da pesquisa
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Genética e causas
O que está alterado no DNA e como passa nas famílias
Nenhum gene associado encontrado
Os dados genéticos desta condição ainda estão sendo catalogados.
Diagnóstico
Os sinais que médicos procuram e os exames que confirmam
Tratamento e manejo
Remédios, cuidados de apoio e o que precisa acompanhar
Onde tratar no SUS
Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)
🇧🇷 Atendimento SUS — Malformação congênita das artérias coronárias
Centros de Referência SUS
24 centros habilitados pelo SUS para Malformação congênita das artérias coronárias
Centros para Malformação congênita das artérias coronárias
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
Hospital Infantil Albert Sabin
R. Tertuliano Sales, 544 - Vila União, Fortaleza - CE, 60410-794 · CNES 2407876
Serviço de Referência
Hospital de Apoio de Brasília (HAB)
AENW 3 Lote A Setor Noroeste - Plano Piloto, Brasília - DF, 70684-831 · CNES 0010456
Serviço de Referência
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
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
Hospital Universitário da UFJF
R. Catulo Breviglieri, Bairro - s/n - Santa Catarina, Juiz de Fora - MG, 36036-110 · CNES 2297442
Atenção Especializada
Hospital das Clínicas da UFMG
Av. Prof. Alfredo Balena, 110 - Santa Efigênia, Belo Horizonte - MG, 30130-100 · CNES 2280167
Serviço de Referência
Hospital Universitário Julio Müller (HUJM)
R. Luis Philippe Pereira Leite, s/n - Alvorada, Cuiabá - MT, 78048-902 · CNES 2726092
Atenção Especializada
Hospital Universitário João de Barros Barreto
R. dos Mundurucus, 4487 - Guamá, Belém - PA, 66073-000 · CNES 2337878
Serviço de Referência
Hospital Universitário Lauro Wanderley (HULW)
R. Tabeliao Estanislau Eloy, 585 - Castelo Branco, João Pessoa - PB, 58050-585 · CNES 0002470
Atenção Especializada
Instituto de Medicina Integral Prof. Fernando Figueira (IMIP)
R. dos Coelhos, 300 - Boa Vista, Recife - PE, 50070-902 · CNES 0000647
Serviço de Referência
Hospital Pequeno Príncipe
R. Des. Motta, 1070 - Água Verde, Curitiba - PR, 80250-060 · CNES 3143805
Serviço de Referência
Hospital Universitário Regional de Maringá (HUM)
Av. Mandacaru, 1590 - Parque das Laranjeiras, Maringá - PR, 87083-240 · CNES 2216108
Atenção Especializada
Hospital de Clínicas da UFPR
R. Gen. Carneiro, 181 - Alto da Glória, Curitiba - PR, 80060-900 · CNES 2364980
Serviço de Referência
Hospital Universitário Pedro Ernesto (HUPE-UERJ)
Blvd. 28 de Setembro, 77 - Vila Isabel, Rio de Janeiro - RJ, 20551-030 · CNES 2280221
Serviço de Referência
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
Hospital São Lucas da PUCRS
Av. Ipiranga, 6690 - Jardim Botânico, Porto Alegre - RS, 90610-000 · CNES 2232928
Serviço de Referência
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
Hospital Universitário da UFSC (HU-UFSC)
R. Profa. Maria Flora Pausewang - Trindade, Florianópolis - SC, 88036-800 · CNES 2560356
Serviço de Referência
Hospital das Clínicas da FMUSP
R. Dr. Ovídio Pires de Campos, 225 - Cerqueira César, São Paulo - SP, 05403-010 · CNES 2077485
Serviço de Referência
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
Hospital de Clínicas da UNICAMP
R. Vital Brasil, 251 - Cidade Universitária, Campinas - SP, 13083-888 · CNES 2748223
Serviço de Referência
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
UNIFESP / Hospital São Paulo
R. Napoleão de Barros, 715 - Vila Clementino, São Paulo - SP, 04024-002 · CNES 2688689
Serviço de Referência
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
Sex Differences in Psychological Distress of Patients With Spontaneous Coronary Artery Dissection (SCAD): The MINDSET Study.
Spontaneous coronary artery dissection (SCAD) is an increasingly recognized cause of acute coronary syndrome, predominantly affecting women. Psychological distress is common pre- and post-SCAD, yet sex-specific patterns remain understudied. This cross-sectional study aimed to examine sex differences in the psychological distress of patients with SCAD. Adult patients diagnosed with SCAD within the past 3 years, confirmed by coronary angiography, were recruited from 6 Canadian hospitals between April 2022 and January 2025. Participants completed questionnaires assessing sociodemographics and validated measures of psychological distress: Patient Health Questionnaire-9 for depression, Generalized Anxiety Disorder-7 for generalized anxiety, Cardiac Anxiety Questionnaire for cardiac-related anxiety, and PTSD Checklist-5 for posttraumatic stress symptoms. Sex differences were analyzed using t tests for continuous variables and χ2 tests for categorical variables. Multivariable linear regression models assessed the association between sex and psychological distress, adjusting for age, pre-SCAD mental health diagnosis, and employment status. Among 326 patients (92.9% women; mean age=53.3±11.1 years), women reported higher rates of preexisting mental health conditions (29.2% versus 8.7%; P=0.035). Post-SCAD women reported higher mean scores than men on the Patient-Health-Questionnaire-9, Cardiac-Anxiety-Questionnaire, and PTSD Checklist-5 (all P<0.05). Female sex was associated with greater depressive (B=2.94; P=0.010), cardiac anxiety (B=7.09; P=0.008), and posttraumatic stress symptoms (B=5.94; P=0.048) after adjustment. Clinically significant symptoms were more common in women versus men: 25.1% versus 0% (depression), 21.5% versus 4.4% (anxiety), 54.8% versus 26.1% (cardiac anxiety), and 15.5% versus 0% (posttraumatic stress). Both women and men experience clinically significant cardiac anxiety following SCAD, but women report a greater psychological burden, including more preexisting mental health conditions and twice the distress after SCAD. These results underscore the importance of routine psychological screening and timely intervention to support mental health and recovery outcomes, particularly among women.
Recognition and treatment of pregnancy-associated spontaneous coronary artery dissection in the postpartum period .
Spontaneous coronary artery dissection (SCAD) is a rare acute coronary artery event; however, it should always be considered in pregnant and postpartum patients as it can be life-threatening if untreated. Diagnosis of pregnancy-associated spontaneous coronary artery dissection (PSCAD) can be challenging when pathophysiological lines are blurred by changes related to pregnancy or concurrent obstetric processes such as pre-eclampsia or haemolysis elevated liver enzymes and low platelets. It has been reported that PSCAD has an increased incidence in women with pre-eclampsia, possibly due to their similar pathogenic mechanisms. We present a case of a woman who developed PSCAD on postpartum day 1 from an uncomplicated vaginal delivery. Her diagnosis was complicated by simultaneous elevation of blood pressures and worsening gestational thrombocytopaenia. The patient underwent coronary artery catheterisation, which confirmed the diagnosis of SCAD and was treated conservatively. She was eventually discharged home without any longstanding complications. .
Unroofed coronary sinus and persistent left superior vena cava: a rare neonatal venous anomaly.
Approach to abnormal cardiovascular signs in the early neonatal period is challenging due to delayed fetal adaptation, closure of the patent ductus arteriosus and physiological immaturity. We present a rare case of unroofed coronary sinus (UCS) with persistent left superior vena cava (PLSVC) in a term neonate who presented with recurrent desaturation episodes and persistent oxygen requirements. Transthoracic echocardiography (TTE) revealed this rare venous anomaly, which is mainly reported in the older population and primarily as an incidental finding. TTE with an agitated saline study was the key diagnostic modality. Early diagnosis is crucial given the potential complications of thromboembolic phenomena and brain abscesses. Clinical suspicion should be high in neonates with persistent unexplained oxygen requirements with a structurally normal heart, primarily when associated with PLSVC. This is the first-ever case report of UCS presenting in the neonatal period.
Genetic Association of Circulating Proteins and Gene Transcripts With Spontaneous Coronary Artery Dissection.
Spontaneous coronary artery dissection (SCAD) is an uncommon cause of myocardial infarction that disproportionately affects women, particularly during pregnancy and the peripartum period. Limited understanding of its underlying pathophysiology hinders the development of effective preventive and therapeutic strategies. This study investigated associations between genetically predicted circulating proteins and tissue-specific RNA levels with genetically predicted SCAD risk using Mendelian randomization and Bayesian colocalization. Genetic scores for >1500 circulating proteins were derived from the UK Biobank (N=34 557) and deCODE (N=35 559). Scores for 13 848 gene transcripts in arterial and fibroblast tissues were generated from Genotype-Tissue Expression data. Associations between these scores and SCAD were assessed in a genome-wide association study meta-analysis of 1917 individuals with SCAD and 9292 controls. Findings were validated in vitro using mass spectrometry-based proteomic analysis of extracellular vesicles from 50 patients with SCAD and 50 healthy controls. Genetic associations of 4 circulating proteins with SCAD (AFAP1 [actin filament-associated protein 1], ECM1 [extracellular matrix protein 1], SPON1 [spondin 1], and STAT6 [signal transducer and activator of transcription 6]) were identified. Two were supported by gene expression data (AFAP1 and ECM1), and one by tissue-specific Bayesian colocalization analyses (ECM1). Protein interaction mapping identified potential shared pathways through the JAK-STAT (Janus kinases and signal transducers and activators of transcription) signaling pathway and inflammatory regulation. Mass spectrometry-based proteomic analysis demonstrated that ECM1 was significantly upregulated in SCAD cases versus controls. Integrative analysis of proteomic, transcriptomic, and experimental data revealed 4 circulating proteins genetically associated with SCAD risk, with ECM1 emerging as a key protein with a likely causal role in SCAD pathogenesis. These findings highlight biological pathways for mechanistic studies and protein targets for potential therapeutic interventions.
Isolated left ventricular apical hypoplasia: a case report.
Isolated left ventricular apical hypoplasia is a rare and lesser-known form of cardiomyopathy characterized by specific findings on cardiac imaging. It is thought to be congenital in origin, with clinical features that can range from being asymptomatic to presenting with heart failure and arrhythmias. A 43-year-old woman presented with chest pain and had previously undergone evaluation at another facility, including a 2D echocardiogram and computed tomography (CT) coronary angiography. These tests revealed a dilated left atrium and ventricle and reduced left ventricular function alongside a Type I left anterior descending artery. A cardiac magnetic resonance image (MRI) and review of the CT scan confirmed a diagnosis of isolated left ventricular apical hypoplasia. Guideline-directed medical therapy was initiated due to the initial presentation of left ventricular dysfunction. Left ventricular apical hypoplasia is characterized by (i) a truncated, spherical, and impaired left ventricle (LV) with bulging of the interventricular septum towards the right ventricle (RV), (ii) fatty material in the apical region of the LV, (iii) abnormalities in the papillary muscles and trabecular structures, and (iv) elongation of the RV wrapping around the underdeveloped LV. Limited data is available on this condition, with only a few reported cases. Currently, no definitive guidelines exist, and management is tailored to the patient's specific presentation, including treating heart failure and any arrhythmias that may arise. While the aetiology of this condition remains poorly understood, it is crucial to recognize it to prevent misdiagnosis and to encourage further research into its management.
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Critical update and discussion of the prevalence, nature, mechanisms of action, and treatment options in potentially serious coronary anomalies.
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Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki)Development and Validation of a Measure of Psychological Distress After Spontaneous Coronary Artery Dissection: The Spontaneous Coronary Artery Dissection Distress Inventory.
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The Journal of international medical researchHalos and Hemoptysis: A Case of Intrapulmonary Sequestration Masquerading as a Pulmonary Aspergilloma.
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Angiologiia i sosudistaia khirurgiia = Angiology and vascular surgeryCoronary Conundrum: Anomalous Pan-Coronary Origin from the Right Sinus with a "Type X" Dual LAD.
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JACC. Cardiovascular interventions[MINOCA revealing an anomalous origin of right coronary artery and a pheochromocytoma : A case report with literature review].
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Zhonghua xin xue guan bing za zhi[Clinical characteristics analysis of 6 children with anomalous origin of coronary artery supported by extracorporeal membrane oxygenation].
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Asian cardiovascular & thoracic annals[Left Coronary Artery Stenosis Long-term After Original Jatene Procedure].
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Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions[Anomalous Origin of the Right Coronary Artery from the Left Sinus of Valsalva Treated with Modified Unroofing Procedure].
Kyobu geka. The Japanese journal of thoracic surgeryAn inadvertently created arteriovenous fistula in the radial artery benefitting the patient for future haemodialysis.
JPMA. The Journal of the Pakistan Medical AssociationCurrent evidence and future directions in antiplatelet therapy for spontaneous coronary artery dissection: balancing ischemic and bleeding risks.
Coronary artery diseasePhoton-counting detector computed tomography compared with cardiac magnetic resonance imaging for myocardial extracellular volume quantification in spontaneous coronary artery dissection.
Scientific reportsHypothyroidism in spontaneous coronary artery dissection: presentation, clinical and angiographic findings, management and outcomes.
Open heartPulmonary Atresia with Intact Ventricular Septum in the Neonate: A Review.
Clinics in perinatologyMyocardial calcification revealed by postmortem computed tomography in a case of infantile myocardial ischemia caused by anomalous origin of the left coronary artery from the pulmonary artery.
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JACC. Case reportsThe Heart's Small Molecules: The Importance of MicroRNAs in Cardiovascular Health.
Journal of clinical medicineMyocardial Ischemia Secondary to Anomalous Origin of Left Anterior Descending Coronary Artery: A Case Report and Literature Review.
The American journal of case reportsAssociation between blood pressure and invasive hemodynamic measures in myocardial bridging.
American journal of physiology. Heart and circulatory physiologyQuantitative evaluation of the myocardial bridge anatomical features and FFRCT in patients with myocardial bridging stratified by age.
MedicineAnomalous left coronary artery from the pulmonary artery in adults: a systematic review of clinical presentation, diagnosis, and outcomes.
The international journal of cardiovascular imagingAnomalous Left Coronary Artery From Pulmonary Artery Masquerading as Myocarditis in an Infant: A Case Report.
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, IncA single-session CT angiography protocol for extracoronary vascular abnormality screening in spontaneous coronary artery dissection (SCAD).
Vascular medicine (London, England)Neoaortic outcomes after the arterial switch operation: A systematic review and meta-analysis.
Archives of cardiovascular diseasesAortic atresia, interrupted hypoplastic right aortic arch, single ventricle and bilateral arterial duct - a unique anatomy with surgical palliation.
Journal of cardiothoracic surgeryUnique Coexistence of Dual Left Anterior Descending Artery and Split Right Coronary Artery.
Methodist DeBakey cardiovascular journalA Meta-Analysis and Simplified Nomenclature for Diagonal Coronary Artery and Ramus Intermedius Across Adult and Pediatric Hearts.
Clinical anatomy (New York, N.Y.)Thrombolysis in Spontaneous Coronary Artery Dissection-Angiographic Findings and Clinical Outcomes.
The Canadian journal of cardiologyComplex Reimplantation of Aneurysmal Left Main Coronary Artery During Reoperative Aortic Root Replacement.
CureusSymptomatic anomalous right coronary artery in mother and daughter, a case report.
Journal of cardiothoracic surgeryUnplanned revascularization and major adverse cardiac events in spontaneous coronary artery disease patients: insights from a cardiac center.
BMC cardiovascular disordersForensic approach in cases of anabolic-androgenic steroid abuse and cardiovascular mortality: insights from autopsy, histopathology, immunohistochemistry and toxicology.
Frontiers in cardiovascular medicineIVUS guiding optimize the outcome of intervention of coronary atherosclerotic stenotic lesions proximal to myocardial bridge.
MedicineEchocardiographic characteristics of 14 cases with uncommon manifestation of Ebstein anomaly in the fetus: a case series report.
Archives of gynecology and obstetricsAtrial septal defect with anomalous coronary: not always a contraindication for device closure.
BMJ case reportsBalloon dilation of the para-device space to alleviate severe flow restriction in an oversized pulmonary flow restrictor: a case report.
BMC cardiovascular disordersCoronary-to-pulmonary artery fistula in a patient with atypical chest pain: case presentation and literature review.
Surgical and radiologic anatomy : SRARemotely delivered mindfulness-based cognitive therapy for spontaneous coronary artery dissection survivors.
Translational behavioral medicineExtra-anatomical ascending-to-descending aortic bypass in an adult patient with aortic coarctation.
Multimedia manual of cardiothoracic surgery : MMCTSClinical features and prognosis in patients with coronary anomalies: the experiences and follow-up results of a single center.
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European heart journal. Case reportsSpontaneous Coronary Artery Dissection: Cardiovascular Events Incidence and Quality of Life Evaluation in a Single-Center 10 Years' Experience.
Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & InterventionsY-Incision Aortic Annular Enlargement in Patients With Anomalous Left Circumflex Artery.
European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic SurgerySurgical Repair of Ruptured Giant Coronary Artery Aneurysm and Pulmonary Artery Fistula.
Interdisciplinary cardiovascular and thoracic surgeryA Rare Congenital Triad in an Adult With Coronary Artery Disease: A Case Report From Georgia.
CureusRecently Developed Undiagnosed Femoral Arteriovenous Fistulas and Cannulation of the Ipsilateral Femoral Vein for Peripheral Cardiopulmonary Bypass in a Patient Undergoing Redo Open Heart Surgery: Perioperative Implications.
Annals of cardiac anaesthesiaRecurrent Chest Pain Due to Spontaneous Coronary Artery Dissection Diagnosed by Optical Coherence Tomography.
Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & InterventionsAnomalous origin of right coronary artery with interarterial and intramural course associated with bicuspid aortic valve and dilation of ascending aorta.
BMJ case reportsA contemporary algorithm to guide percutaneous coronary intervention in high-risk spontaneous coronary artery dissection.
The Journal of invasive cardiologyTranscatheter closure of multiple coronary to pulmonary artery fistulas in Fontan physiology using Amplatzer Vascular Plugs.
Cardiology in the youngA case of coronary sinus ostium atresia with muscular obstruction in a complex univentricular heart managed in stages.
Cardiology in the youngAnomalous Origin of the Left Coronary Artery from the Pulmonary Artery Syndrome in Adults: A Case-Based Clinical Review.
Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidirClarifying the Cardiovascular Morphology and Associated Abnormalities in Patients with Double Inlet Left Ventricle Using Multidetector CT Angiography.
Pediatric cardiologyOptimising pre-operative assessment in double-outlet right ventricle: the complementary role of echocardiography and CT angiography.
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CirculationAtypical presentation of ALCAPA in a young boy: a case report.
Cardiology in the youngDiagnosis of Coronary Artery Aneurysm in a Caucasian Population Cohort: Evaluating the Agreement Between Japanese Criteria and Different Z Score Formulas.
Journal of clinical medicineAn autopsy case of eosinophilic coronary periarteritis with coronary arterial degeneration and repaired dissection.
Journal of forensic and legal medicineClinical and Prognostic Significance of Anomalous Origin of a Coronary Artery in Adults.
CirculationDiagnostic performance of coronary CT angiography to diagnose acute spontaneous coronary artery dissection.
Journal of cardiovascular computed tomographyA Systematic Analysis of Coronary to Pulmonary Artery Fistula and Its Associated Aneurysm in Adults.
Interdisciplinary cardiovascular and thoracic surgeryPercutaneous closure of a large left main coronary artery fistula in a paediatric patient.
Cardiology in the youngElements of Complexity in the Surgical Anatomy of Laparoscopic Median Arcuate Ligament Release.
The American surgeonHypercholesterolemic valvulopathy and severe atherosclerosis in paediatric patients.
Cardiology in the youngTotally anomalous origin of the coronary arteries from the pulmonary trunk: a case report.
Cardiology in the youngAutomated intravascular ultrasound image processing and quantification of coronary artery anomalies: The AIVUS-CAA software.
Computer methods and programs in biomedicineA Novel Classification Proposal for Iatrogenic Arteriovenous Fistulas and Pseudoaneurysms After Transfemoral Cardiovascular Interventions-An Analysis of a Single-Center Database of 5941 Punctures.
Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & InterventionsA Rare Cardiac Malformation: Isolated Double-Orifice Mitral Valve.
Echocardiography (Mount Kisco, N.Y.)Prenatal Diagnosis of Fetal Heart Malformation With Abnormal Number of Pulmonary Artery Branches as the Initial Clue.
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in MedicineUpper Extremity Variant Vascular Anatomy: Navigation Techniques.
Interventional cardiology clinicsPersonalized External Aortic Root Support (PEARS) in the Treatment of Marfan Syndrome and Bicuspid Aortic Valve Aneurysms: First Case Series in the American Continent.
Brazilian journal of cardiovascular surgerySurgical Results for Anomalous Aortic Origin of Coronary Artery - Is Right Side Prompt Surgery Necessary?
Circulation journal : official journal of the Japanese Circulation SocietyUnusual Revelation of an Anomalous Right Coronary Artery: Non-ST Segment Elevation Myocardial Infarction (NSTEMI) in the Context of Drug Abuse.
CureusProximal Left Coronary Artery Occlusion After Transcatheter Pulmonary Valve Implantation With Self-Expanding VenusP-Valve: A Case Report.
Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & InterventionsMinimally invasive surgical repair of an aneurysmal coronary-pulmonary artery fistula.
Multimedia manual of cardiothoracic surgery : MMCTSHigh incidence of adverse events in spontaneous coronary artery dissection patients during mid-term follow-up: a persistent challenge ahead.
Minerva cardiology and angiologyPaediatric scoring systems in congenital heart surgery: evaluating predictive accuracy for major adverse events.
Cardiology in the youngNoninvasive Anatomical and Functional Imaging for Hemodynamic Relevance in Right Coronary Artery Anomalies.
JAMA cardiologyAortocoronary flap technique in arterial switch for single coronary: Two case reports.
Science progressUnmasking Myocardial Bridge-Related Ischemia by Quantitative Flow Ratio Functional Evaluation.
The American journal of cardiologyConservative Management of Giant Aneurysm of the Left Main to Left Circumflex Arteries.
JACC. Case reportsExtracoronary Arterial Pathologies in Patients With Spontaneous Coronary Artery Dissection.
The American journal of cardiologyPrognostic Significance of aVR Lead and QTc Prolongation in Patients with Early Repolarization.
Medicina (Kaunas, Lithuania)Myocardial Infarction in Young Adults: A Case Series and Comprehensive Review of Molecular and Clinical Mechanisms.
BiomoleculesMultimodal imaging in young male with bicuspid aortic valve, right-sided aorto-atrial fistula and single coronary artery.
Cardiovascular ultrasoundAn in-depth analysis of coronary computed tomography angiography segmental findings in acute spontaneous coronary artery dissection - a prospective multicenter study.
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The international journal of cardiovascular imagingA Rare Case of Undiagnosed Anomalous Right Coronary Artery From the Pulmonary Artery in an Asymptomatic Seven-Year-Old.
World journal for pediatric & congenital heart surgeryAnomalous Single Ostial Origin of Entire Coronary Arteries From the Right Coronary Sinus: A Rare Case of ST-Segment Elevation Myocardial Infarction Treated With Primary Percutaneous Coronary Intervention.
Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & InterventionsImpact of Myocardial Bridging on Hemodynamics Evaluated by Coronary Angiography-Derived Fractional Flow Reserve.
The American journal of cardiologyExercise stress cardiovascular magnetic resonance imaging is feasible in adolescents and young adults with anomalous coronary arteries.
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Annals of pediatric cardiologyDeveloping a reduced order model for pulsatile blood flow simulations using minimal three-dimensional simulation data.
Computer methods and programs in biomedicineA rare coronary artery anomaly: abnormal single coronary artery from pulmonary artery.
Cardiology in the youngReevaluating the diagnosis of right coronary artery absence: A thoughtful analysis of a case report.
MedicineIatrogenic anastomosis of the internal mammary artery with the great cardiac vein: The first documented case report in Palestine with a literature review.
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Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & InterventionsLeft circumflex artery occlusion during aortic valvuloplasty in a young patient with bicuspid aortic valve: a case report.
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JACC. Case reportsAssociações
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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.
- Sex Differences in Psychological Distress of Patients With Spontaneous Coronary Artery Dissection (SCAD): The MINDSET Study.
- Recognition and treatment of pregnancy-associated spontaneous coronary artery dissection in the postpartum period  .
- Unroofed coronary sinus and persistent left superior vena cava: a rare neonatal venous anomaly.
- Genetic Association of Circulating Proteins and Gene Transcripts With Spontaneous Coronary Artery Dissection.
- Isolated left ventricular apical hypoplasia: a case report.
- Prevalence and spectrum of coronary artery anomalies detected on coronary CT angiography.
- Micro-coil embolization for transcatheter septal ablation in a hypertrophic obstructive cardiomyopathy patient and an unusual coronary anatomy: a case report.
- 'X-cross' left coronary artery congenital anomaly.
- Critical update and discussion of the prevalence, nature, mechanisms of action, and treatment options in potentially serious coronary anomalies.
- Congenital right coronary artery-to-right ventricular outflow tract fistula device closure with migration: retrieval of device after eight years.
Bases de dados e fontes oficiais
Identificadores e referências canônicas usadas para montar este verbete.
- ORPHA:1081(Orphanet)
- MONDO:0015203(MONDO)
- GARD:1534(GARD (NIH))
- Busca completa no PubMed(PubMed)
- Q5172184(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
