Polydactyly and Single Umbilical Artery: Lesser Known Associations with Beckwith–Weidemann Syndrome
Background: Beckwith–Wiedemann syndrome (BWS) is the most common genetic overgrowth syndrome characterized by the triad of macroglossia, macrosomia, and abdominal wall defects. Clinical Description: We report the case of a term baby girl who was born with mesoaxial polydactyly of her left foot. Ther...
Main Author: | Deepika Rustogi |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2022-01-01
|
Series: | Indian Pediatrics Case Reports |
Subjects: | |
Online Access: | http://www.ipcares.org/article.asp?issn=2772-5170;year=2022;volume=2;issue=3;spage=182;epage=185;aulast=Rustogi |
Similar Items
-
Unilateral testicular enlargement in a teenager with Beckwith-Wiedemann syndrome: a case report
by: Maria Chiara Pellegrin, et al.
Published: (2019-07-01) -
Two Infants with Beckwith-Wiedemann Syndrome
by: Ratbi I, et al.
Published: (2010-01-01) -
SHORT RIB POLYDACTYLY SYNDROME
by: Z Moinfar, et al.
Published: (2007-09-01) -
SHORT RIB POLYDACTYLY SYNDROME
by: Z Moinfar, et al.
Published: (2007-12-01) -
Guided Wave Transducer for the Locating Defect of the Steel Pipe Based on the Weidemann Effect
by: Jin Xu, et al.
Published: (2021-12-01)