Glycogen storage disease type I epidemiology and demographics: Difference between revisions
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{{Glycogen storage disease type I}} | {{Glycogen storage disease type I}} | ||
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==Overview== | ==Overview== | ||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
GSD Ia has an [[incidence]] in the American population of approximately 1 in 100,000 to 200,000 births. None of the glycogenoses are currently detected by standard or extended [[newborn screening]]. | GSD Ia has an [[incidence]] in the American population of approximately 1 in 100,000 to 200,000 births. None of the glycogenoses are currently detected by standard or extended [[newborn screening]]. | ||
==References== | ==References== | ||
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[[Category:Metabolic disorders]] | [[Category:Metabolic disorders]] | ||
[[Category:Mature chapter]] | [[Category:Mature chapter]] | ||
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Revision as of 00:07, 20 September 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
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Overview
Epidemiology and Demographics
GSD Ia has an incidence in the American population of approximately 1 in 100,000 to 200,000 births. None of the glycogenoses are currently detected by standard or extended newborn screening.