DIRETRIZES

  1. Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases (link)

  2. ACMG Standards and Guidelines for the Interpretation of Sequence Variants: A Joint Consensus Recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology (link)

  3. Guideline ACMG Evaluation of Cardiomyopathy (link)

  4.  2017. AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death (link)

  5. Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases (link)

  6. 2019. HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy (link)

  7. Genetic Abnormalities of the Sinoatrial Node and Atrioventricular Conduction (link)

  8. 2014. ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy (link)

  9. HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes (link)

  10. 2022. AHA/ACC/HFSA Guideline for the Management of Heart Failure: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines (link)

  11. Guidelines and new directions in the therapy and monitoring of ATTRv amyloidosis (link)

  12. Malaquias AC, Ferreira LV, Souza SC, Arnhold IVP, Mendonça BB, Jorge AAL. Síndrome de Noonan: do fenótipo à terapêutica com hormônio de crescimento. Arq Bras Endocrinol Metab 2008; 52(5). (link)

  13. Sousa VC, Fonseca IM, Cordeiro A, Lopes MJP. Manifestações cutâneas das Rasopatias. J Port Soc Dermat 2017; 75(1):9-18. (link)

  14. Marcondes-Braga FG, Moura LAZ, Issa VS, Vieira JL, Rohde LE, Simões MV, et al. Atualização de Tópicos Emergentes da Diretriz de Insuficiência Cardíaca – 2021. Arq Bras Cardiol. 2021; 116(6):1174-1212. (link)

  15. Saliba A, Figueiredo AC, Baroneza JE, Afiune JY, Pic-Taylor A, Oliveira SF, et al. Genética e genônimica na cardiopatia congênita: uma revisão clínica. J Pediatr (Rio J). 2020;96:279-88. (link)

  16. SOBRAC – Hachul DT, Kunioyshi RR, Darrieux FCC. Tratado de Arritmias cardíacas: fisiopatologia, diagnóstico e tratamento. 1ª ed. São Paulo: Atheneu, 2020. (link)

  17. Magalhães LP, Guimarães ICB, Melo SL, Mateo EIP, Andalaft RB, Xavier LFR, et al. Diretriz de Arritmias Cardíacas em Crianças e Cardiopatias Congênitas SOBRAC e DCC – CP. Arq Bras Cardiol 2016; 107(1Supl.3):1-58. (link)

  18. Coelho SG, Almeida AG. Síndrome de Marfan revisitada – da genética à clínica. Rev Port Cardiol 2016; 39(4):215-226. (link)

  19. Graffunder FP, Sties SW, Gonzales AI, Carvalho T. Diagnóstico diferencial de Síndrome de Marfan em adolescente atleta de voleibol. Int J Cardiovasc Sci 2017; 30(2). (link)