Details

Autor(en) / Beteiligte

• Allanson, Judith E.

Titel

Noonan syndrome

Ist Teil von

• American journal of medical genetics. Part C, Seminars in medical genetics, 2007-08, Vol.145C (3), p.274-279

Ort / Verlag

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

Erscheinungsjahr

2007

Quelle

MEDLINE

Beschreibungen/Notizen

• Noonan syndrome is a common autosomal dominant condition caused by multiple genes in the RasMAPK pathway. The adult phenotype can be extremely subtle, and many adults are diagnosed only after the birth of a more obviously affected child. Whether diagnosis is made in childhood or adulthood, initial and ongoing evaluation of many systems can have considerable health benefits. © 2007 Wiley‐Liss, Inc.