Progeria epidemiology and demographics: Difference between revisions

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===Race===
===Race===


*[Disease name] usually affects individuals of the [race 1] race. [Race 2] individuals are less likely to develop [disease name].
*There is no [[race]] predilection of [[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) till now.
===Gender===
===Gender===
*[[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) affects men and women equally but males are little more commonly affected by [[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) than females.  
*[[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) affects men and women equally but males are little more commonly affected by [[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) than females.  

Revision as of 14:23, 17 July 2019

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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

Prevalence

Age

Race

Gender

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].

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References

  1. Hennekam RC (2006). "Hutchinson-Gilford progeria syndrome: review of the phenotype". Am J Med Genet A. 140 (23): 2603–24. doi:10.1002/ajmg.a.31346. PMID 16838330.
  2. Hennekam RC (2006). "Hutchinson-Gilford progeria syndrome: review of the phenotype". Am J Med Genet A. 140 (23): 2603–24. doi:10.1002/ajmg.a.31346. PMID 16838330.
  3. Hennekam RC (2006). "Hutchinson-Gilford progeria syndrome: review of the phenotype". Am J Med Genet A. 140 (23): 2603–24. doi:10.1002/ajmg.a.31346. PMID 16838330.
  4. Hennekam RC (2006). "Hutchinson-Gilford progeria syndrome: review of the phenotype". Am J Med Genet A. 140 (23): 2603–24. doi:10.1002/ajmg.a.31346. PMID 16838330.

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