Noonan syndrome epidemiology and demographics: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Noonan syndrome}} | {{Noonan syndrome}} | ||
{{CMG}}; {{AE}} Serge Korjian | {{CMG}}; {{AE}} [[User:Sergekorjian|Serge Korjian]], [[User:YazanDaaboul|Yazan Daaboul]] | ||
==Overview== | ==Overview== | ||
The estimated prevalence of Noonan Syndrome in the general population is 1 in 1000 to 2500 individuals with equal male to female ratio. | |||
== | ==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.<ref name="pmid3895929">{{cite journal| author=Mendez HM, Opitz JM| title=Noonan syndrome: a review. | journal=Am J Med Genet | year= 1985 | volume= 21 | issue= 3 | pages= 493-506 | pmid=3895929 | doi=10.1002/ajmg.1320210312 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3895929 }} </ref> | |||
==References== | ==References== | ||
{{Reflist| | {{Reflist|1}} | ||
{{Phakomatoses and other congenital malformations not elsewhere classified}} | {{Phakomatoses and other congenital malformations not elsewhere classified}} | ||
Latest revision as of 02:24, 9 November 2013
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Serge Korjian, Yazan Daaboul
Overview
The estimated prevalence of Noonan Syndrome in the general population is 1 in 1000 to 2500 individuals with equal male to female ratio.
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