Glycogen storage disease type II epidemiology and demographics: Difference between revisions
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* | *Glycogen storage disease type II usually affects individuals of the Caucasian race.<ref name="pmid16737883">{{cite journal| author=Kishnani PS, Hwu WL, Mandel H, Nicolino M, Yong F, Corzo D et al.| title=A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease. | journal=J Pediatr | year= 2006 | volume= 148 | issue= 5 | pages= 671-676 | pmid=16737883 | doi=10.1016/j.jpeds.2005.11.033 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16737883 }} </ref> | ||
===Gender=== | ===Gender=== | ||
*Glycogen storage disease type II affects men and women equally. | *Glycogen storage disease type II affects men and women equally. |
Revision as of 17:27, 11 January 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Anmol Pitliya, M.B.B.S. M.D.[2]
Overview
Epidemiology and Demographics
Incidence
- The incidence of glycogen storage disease type 2 (GSD type 2) is approximately 11.5 per 100,000 individuals in the state of Illinois, United States.[1]
- The predicted incidence of glycogen storage disease type 2 is approximately 2.5 per 100,000 individuals in Netherlands. This incidence in divided into 0.7 per 100,000 individuals for infantile GSD type 2 and 1.8 per 100,000 individuals for adult GSD type 2.[2]
Prevalence
- The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
- In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide.
- The prevalence of [disease/malignancy] is estimated to be [number] cases annually.
Case-fatality rate/Mortality rate
- In [year], the incidence of [disease name] is approximately [number range] per 100,000 individuals with a case-fatality rate/mortality rate of [number range]%.
- The case-fatality rate/mortality rate of [disease name] is approximately [number range].
Age
- Patients of all age groups may develop [disease name].
- The incidence of [disease name] increases with age; the median age at diagnosis is [#] years.
- [Disease name] commonly affects individuals younger than/older than [number of years] years of age.
- [Chronic disease name] is usually first diagnosed among [age group].
- [Acute disease name] commonly affects [age group].
Race
- Glycogen storage disease type II usually affects individuals of the Caucasian race.[3]
Gender
- Glycogen storage disease type II affects men and women equally.
Region
- The majority of [disease name] cases are reported in [geographical region].
- [Disease name] is a common/rare disease that tends to affect [patient population 1] and [patient population 2].
Developed Countries
Developing Countries
References
- ↑ Burton BK, Charrow J, Hoganson GE, Waggoner D, Tinkle B, Braddock SR; et al. (2017). "Newborn Screening for Lysosomal Storage Disorders in Illinois: The Initial 15-Month Experience". J Pediatr. 190: 130–135. doi:10.1016/j.jpeds.2017.06.048. PMID 28728811.
- ↑ Ausems MG, Verbiest J, Hermans MP, Kroos MA, Beemer FA, Wokke JH; et al. (1999). "Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling". Eur J Hum Genet. 7 (6): 713–6. doi:10.1038/sj.ejhg.5200367. PMID 10482961.
- ↑ Kishnani PS, Hwu WL, Mandel H, Nicolino M, Yong F, Corzo D; et al. (2006). "A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease". J Pediatr. 148 (5): 671–676. doi:10.1016/j.jpeds.2005.11.033. PMID 16737883.