Noonan syndrome epidemiology and demographics
Noonan syndrome Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Noonan syndrome epidemiology and demographics On the Web |
American Roentgen Ray Society Images of Noonan syndrome epidemiology and demographics |
Risk calculators and risk factors for Noonan syndrome epidemiology and demographics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Serge Korjian, Yazan Daaboul
Overview
Epidemiology and Demographics
Noonan syndrome is inherited in an autosomal dominant pattern, and despite the disease being congenital, it can manifest at different ages due to its variable expression. In general, males and females have the same incidence of the disease which can be explained by the inheritance pattern. The estimated prevalence in the general population is 1 in 1000 to 2500 individuals.[1]
References
- ↑ Mendez HM, Opitz JM (1985). "Noonan syndrome: a review". Am J Med Genet. 21 (3): 493–506. doi:10.1002/ajmg.1320210312. PMID 3895929.
Template:Phakomatoses and other congenital malformations not elsewhere classified