Noonan syndrome overview: Difference between revisions
Gerald Chi (talk | contribs) (Created page with "__NOTOC__ {{Noonan syndrome}} {{CMG}} ==Overview== Noonan Syndrome (NS) is a relatively common congenital genetic condition which affects both males and females. It used ...") |
No edit summary |
||
| Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{Noonan syndrome}} | {{Noonan syndrome}} | ||
{{CMG}} | {{CMG}}; {{AE}} {{AO}} | ||
==Overview== | ==Overview== | ||
Revision as of 22:25, 18 August 2013
|
Noonan syndrome Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Noonan syndrome overview On the Web |
|
American Roentgen Ray Society Images of Noonan syndrome overview |
|
Risk calculators and risk factors for Noonan syndrome overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ayokunle Olubaniyi, M.B,B.S [2]
Overview
Noonan Syndrome (NS) is a relatively common congenital genetic condition which affects both males and females. It used to be referred to as the male version of Turner's syndrome[1]; however, the genetic causes of Noonan syndrome and Turner syndrome are distinct. The principal features include congenital heart malformation, short stature, learning problems, indentation of the chest, impaired blood clotting, and a characteristic configuration of facial features. The syndrome is named after Dr Jacqueline Noonan.
It is believed that between approximately 1 in 1,000 and 1 in 2,500 children worldwide are born with NS. It is one of the most common genetic syndromes associated with congenital heart disease, similar in frequency to Down syndrome. However, the range and severity of features can vary greatly in patients with NS. Therefore, the syndrome is not always identified at an early age.
References
Template:Phakomatoses and other congenital malformations not elsewhere classified