Prenatal diagnosis of Greig cephalopolysyndactyly syndrome: a case report

• Type: Article in International Scientific Journal
• Date: 2015

Authors

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

Journal

Title: Prenatal Diagnosis

Vol. 35

Pages: 203-205

ISSN: 0197-3851

Publisher: Wiley-Blackwell

Indexing

ISI Web of Knowledge - 0 Citations

Scopus - 2 Citations

Other information

Authenticus ID: 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.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 3