Syndromes and Disorders Associated with Omphalocele (I): Beckwith–Wiedemann Syndrome

Syndromes and Disorders Associated with Omphalocele (I): Beckwith–Wiedemann Syndrome

Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is characterized by macrosomia, macroglossia, visceromegaly, hemihypertrophy, abdominal wall defects, ear creases/pits, neonatal hypoglycemia, polyhydramnios, placentomegaly, placental mesenchymal dysplasia, cardiac defects, nevus flammeus, hemangiomata...

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Bibliographic Details
Main Author: Chih-Ping Chen
Format: Article
Language:English
Published: Elsevier 2007-06-01
Series:Taiwanese Journal of Obstetrics & Gynecology
Subjects:
Beckwith–Wiedemann syndrome
genetics
omphalocele
Online Access:http://www.sciencedirect.com/science/article/pii/S1028455907600023

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http://www.sciencedirect.com/science/article/pii/S1028455907600023

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