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Split Hand/Foot Malformation: Case Series A Case Report and Review of Literature

Authors :
Divya Chauhan
Alpana Singh
Source :
Journal of Clinical and Diagnostic Research, Vol 13, Iss 1, Pp QD05-QD06 (2019)
Publication Year :
2019
Publisher :
JCDR Research and Publications Private Limited, 2019.

Abstract

Split Hand/Foot Malformation (SHFM) is a rare genetic disorder. It is also known as ectrodactyly. In this disorder, the central rays of the hand and feet are affected leading to various malformations of the hands and feet. Any number of limbs can be affected. It can present in isolation affecting only the limbs or it can be associated with the syndrome. The prevalence of this malformation is 0.06 per 1000 total births. Here, authors report a case in which a pregnant patient had SHFM and the fetus also suffered the same anomaly. The anomaly was detected on ultrasound and medical termination of pregnancy was done.

Details

Language :
English
ISSN :
2249782X, 0973709X, and 41895487
Volume :
13
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Journal of Clinical and Diagnostic Research
Publication Type :
Academic Journal
Accession number :
edsdoj.be696d41895487bad674f05161b3513
Document Type :
article
Full Text :
https://doi.org/10.7860/JCDR/2019/38303.12490