Noonan syndrome: A case report

Noonan syndrome is a developmental disorder characterized by facial dysmorphia, short stature, cardiac defects and skeletal malformations. It may be sporadic or inherited as an autosomal dominant or recessive trait and occurs, one in 1000-2500 children. This is a case report of a 13 year-old girl wh...

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Bibliographic Details
Main Authors: Asokan S, Muthu M, Rathna Prabhu V
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2007-09-01
Series:Journal of Indian Society of Pedodontics and Preventive Dentistry
Subjects:
Online Access:http://www.jisppd.com/article.asp?issn=0970-4388;year=2007;volume=25;issue=3;spage=144;epage=147;aulast=Asokan