Relato de caso: Embriopatia por varfarina - uma síndrome congênita prevenível

Authors

DOI:

https://doi.org/10.12662/1809-5771ri.128.5063.p61-63.2025

Keywords:

Aconselhamento Genético, Desenvolvimento Embrionário, Teratogênese, Varfarina

Abstract

Abstract

Warfarin embryopathy is a pathology that causes bone and nerve malformations in the fetus, due to warfarin use during pregnancy. This study aims to present a case report on warfarin embryopathy, in view of the scarcity in the literature. Case report: Patient, 8 months old, female, admitted to the Genetics outpatient clinic due to nasal hypoplasia and report of the mother who used Warfarin during pregnancy. Final considerations: Warfarin syndrome is a rare pathology, with clinical diagnosis and imaging, which requires a multidisciplinary and longitudinal treatment.

Keywords:Genetic Counseling, Embryonic Development, Teratogenesis, Warfarin

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Author Biographies

João Paulo Farias da Silveira, Unichristus

Building Technician from the Federal Institute of Education, Science and Technology of Ceará (IFCE) (Graduated in 2018). Graduate in Medicine at UNICHRISTUS (Sixth semester) (2023.2). Volunteer Participant of the Therapeutic Toy Extension Project at the Federal University of Ceará (UFC). Effective Participant of the UNICHRISTUS Gastroenterology League (@Ligastro). Scholarship Participant of the Scientific Initiation on Craniofacial Anomalies.

Sara Silveira Brandão, UNICHRISTUS

Medical Student at Centro Universitário Christus. Human Anatomy Monitor, effective member of a scientific initiation in Genetic Counseling and research volunteer on the correlation between COVID-19 and sarcopenia. Active member of the Academic League of Orthopedics, active member of IFMSA Unichristus

Maria Clara Duarte de Figueirêdo, UNICHRISTUS

Medical student at Centro Universitário Christus (Unichristus). Working mainly on the following topics: anthropometry, vital signs, elderly, health and medicine. Member of the Therapeutic Toy extension project: Anatomy as a tool to promote the health of children with cancer, by the Federal University of Ceará (UFC) and Vice-President of the Gastroenterology League: Extension with an approach to gastrointestinal diseases in the community, by the University Center Christus (Unichristus). Developing research in the Geriatric area, in the line of research on Vascular Dementia and in the Pediatric area on the child and youth development of individuals undergoing cancer treatment.

Wallace William da Silva Meireles , Medico Geneticista do Hospital Infantil Albert Sabin (HIAS)

Graduação em Medicina pela Universidade Federal do Ceará (2016). Residência Médica em Genética Médica pela Secretaria Estadual de Saúde do Distrito Federal (2023). Título de Especialista em Pediatria pela Associação Médica Brasileira e Sociedade Brasileira de Pediatria (2021). Especialização em Saúde da Família pela Universidade Federal do Ceará (2018). 

Erlane Marques Ribeiro , Medica Geneticista do Hospital Infantil Albert Sabin (HIAS)

Possui graduação em Medicina pela Universidade Federal do Ceará (1989), mestrado em Medicina (Pediatria) pela Universidade de São Paulo (1997) e doutorado em Ciências da Saúde pela Universidade Federal do Rio Grande do Norte (2014). Membro titular da sociedade brasileira de pediatria e sociedade brasileira de genetica medica. Atualmente é médica neonatologista do Hospital Geral de Fortaleza e geneticista do Hospital Infantil Albert Sabin do Governo do Estado do Ceará, professora da Genética Médica da Faculdade de Medicina Unichristus, diretora do Instituto de Pesquisa , Ensino e Extensão em Ciências da Saúde . Tem experiência na área de Medicina, com ênfase em Genética e Pediatria, atuando principalmente nos seguintes temas: genetica e saude publica, diagnóstico e tratamento de doenças genéticas, aconselhamento genético e erros inatos do metabolismo

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Published

2025-06-20

Issue

No. 128 (2025): Ed. Suplementar

Section

Relatos de Caso/Experiência

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