Review: Noonan syndrome
Source: Lancet
Area: News
Noonan syndrome is a genetic multisystem disorder characterised by distinctive facial features, developmental delay, learning difficulties, short stature, congenital heart disease, renal anomalies, lymphatic malformations, and bleeding difficulties. This review discusses the signs and symptoms of the disease, natural history, diagnosis, and management and differential diagnosis.
Source: NeLM - News - Category: Drugs & Pharmacology Source Type: news
More News: Bleeding | Cardiology | Drugs & Pharmacology | Genetics | Heart | Heart Disease | Learning | Noonan Syndrome | Universities & Medical Training