Noonan syndrome – a new survey

Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genetic features. Various symptoms have been reported for this abnormality such as short stature, unusual facial characteristics, congenital heart abnormalities, developmental complications, and an elevate...

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Bibliographic Details
Main Authors: Alireza Tafazoli, Peyman Eshraghi, Zahra Kamel Koleti, Mohammadreza Abbaszadegan
Format: Article
Published: Termedia Publishing House 2016-12-01
Series:Archives of Medical Science
Online Access:,19,28939,1,1.html