Crouzon syndrome

Crouzon syndrome

Crouzon syndrome is an autosomal dominant disorder with complete penetrance and variable expressivity. Described by a French neurosurgeon in 1912, it is a rare genetic disorder. Crouzon syndrome is caused by mutation in the fibroblast growth factor receptor 2 (FGFR2) gene. Normally, the sutures in t...

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Bibliographic Details
Main Authors: Neha Rajappa, Sadananda Patra, Abha Gahlot, Snehal Bhalsing
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2013-01-01
Series:Medical Journal of Dr. D.Y. Patil University
Subjects:
Crouzon syndrome
fibroblast growth factor
premature synostosis
Online Access:http://www.mjdrdypu.org/article.asp?issn=0975-2870;year=2013;volume=6;issue=3;spage=321;epage=323;aulast=Rajappa

Internet

http://www.mjdrdypu.org/article.asp?issn=0975-2870;year=2013;volume=6;issue=3;spage=321;epage=323;aulast=Rajappa

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