Prenatal diagnosis of Greig cephalopolysyndactyly syndrome: a case report

• Tipo: Artigo em Revista Científica Internacional
• Data: 2015

Autores

Raposo, L (Autor) Outra; Fachada, H (Autor) Outra; Paulo, AS (Autor) Outra; Cerveira, I (Autor) Outra; CASTEDO, S (Autor) FMUP; Pereira, S (Autor) Outra

Revista

Título: Prenatal Diagnosis

Vol. 35

Páginas: 203-205

ISSN: 0197-3851

Editora: Wiley-Blackwell

Indexação

ISI Web of Knowledge - 0 Citações

Scopus - 2 Citações

Outras Informações

ID Authenticus: P-00A-5A3

DOI: 10.1002/pd.4506

Abstract (EN): What's already known about this topic? Greig cephalopolysyndactyly syndrome (GCPS) is a rare multiple congenital anomaly syndrome with an autosomal dominant pattern of inheritance. Prenatal diagnosis is challenging because the ultrasound findings are relatively non-specific. What does this study add? Prenatal diagnosis of GCPS is difficult but possible. Ultrasound findings and family history play the main role that can lead to this diagnosis as in this case. © 2014 John Wiley & Sons, Ltd.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 3