Phenylketonuria epidemiology and demographics: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Phenylketonuria}} | {{Phenylketonuria}} | ||
{{CMG}}; {{AE}} | |||
{{CMG}} {{AE}} | |||
==Overview== | ==Overview== | ||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
===Incidence=== | |||
The [[incidence (epidemiology)|incidence]] of PKU is about 1 in 15,000 births, but the incidence varies widely in different human populations from 1 in 4,500 births among the population of Ireland<ref>{{cite journal | author=DiLella, A. G., Kwok, S. C. M., Ledley, F. D., Marvit, J., Woo, S. L. C. | year=1986 | title=Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene | journal=Biochemistry | volume=25 | pages=743-749 | id=PMID 3008810}}</ref> to fewer than one in 100,000 births among the population of Finland.<ref>{{cite journal | author=Guldberg, P., Henriksen, K. F., Sipila, I., Guttler, F., de la Chapelle, A. | year=1995 | title=Phenylketonuria in a low incidence population: molecular characterization of mutations in Finland | journal=J. Med. Genet | volume=32 | pages=976-978 | id=PMID 8825928}}</ref> | |||
===Gender=== | |||
===Race=== | |||
===Developed Countries=== | |||
===Developing Countries=== | |||
==References== | ==References== | ||
{{Reflist|2}} | |||
{{ | [[Category:Pediatrics]] | ||
[[Category:Neurology]] | |||
[[Category:Endocrinology]] | |||
{{WS}} | |||
{{WH}} | |||
Latest revision as of 13:12, 26 July 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Epidemiology and Demographics
Incidence
The incidence of PKU is about 1 in 15,000 births, but the incidence varies widely in different human populations from 1 in 4,500 births among the population of Ireland[1] to fewer than one in 100,000 births among the population of Finland.[2]
Gender
Race
Developed Countries
Developing Countries
References
- ↑ DiLella, A. G., Kwok, S. C. M., Ledley, F. D., Marvit, J., Woo, S. L. C. (1986). "Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene". Biochemistry. 25: 743–749. PMID 3008810.
- ↑ Guldberg, P., Henriksen, K. F., Sipila, I., Guttler, F., de la Chapelle, A. (1995). "Phenylketonuria in a low incidence population: molecular characterization of mutations in Finland". J. Med. Genet. 32: 976–978. PMID 8825928.