<i>Hutchinson-Gilford syndrome</i> (progeria)

Progeria is a rare, autosomal dominant, progeroid disorder. In the world literature less than 100 cases have been reported to date. We present this case because of its rarity.

Bibliographic Details
Main Authors: Surjushe Amar, Thakre Minal, Vasani Resham, Saple Dattatray
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2009-01-01
Series:Indian Journal of Dermatology
Subjects:
Online Access:http://www.e-ijd.org/article.asp?issn=0019-5154;year=2009;volume=54;issue=5;spage=27;epage=28;aulast=Surjushe