Goltz syndrome: A newborn with ectrodactyly and skin lesions

Goltz syndrome or Focal Dermal Hypoplasia is a rare multisystem disorder, involving all the three germ cell layers. The disease is thought to be inherited in X-linked dominant fashion with heterogeneous mutations of the PORCN gene at Xp11.23 locus. Majority of the cases are sporadic, mainly due to p...

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Bibliographic Details
Main Authors: Shatanik Sarkar, Chaitali Patra, Amit Das, Sutirtha Roy
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2015-01-01
Series:Indian Journal of Dermatology
Subjects:
Online Access:http://www.e-ijd.org/article.asp?issn=0019-5154;year=2015;volume=60;issue=2;spage=215;epage=215;aulast=Sarkar