Progeria epidemiology and demographics: Difference between revisions

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{{Progeria}}
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==Overview==
==Overview==
[[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) is an extremely rare [[Heredity|hereditary]] disease. The [[incidence]] of [[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) is very rare. The usual age of [[diagnosis]] for [[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) ia around two to three years of age. Approximately 100 cases of [[Hutchinson-Gilford progeria syndrome]] (HGPS) have been reported in the literature till now worldwide.


==Epidemiology and Demographics==
==Epidemiology and Demographics==
===Incidence===
===Incidence===
*The incidence of Hutchinson-Gilford progeria syndrome (HGPS) is approximately one in four to eight million births.
*The [[incidence]] of [[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) is approximately one in four to eight million births worldwide.<ref name="pmid16838330">{{cite journal| author=Hennekam RC| title=Hutchinson-Gilford progeria syndrome: review of the phenotype. | journal=Am J Med Genet A | year= 2006 | volume= 140 | issue= 23 | pages= 2603-24 | pmid=16838330 | doi=10.1002/ajmg.a.31346 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16838330  }}</ref><ref name="pmid21251803">{{cite journal| author=Doubaj Y, Lamzouri A, Elalaoui SC, Laarabi FZ, Sefiani A| title=[Three cases of Hutchinson-Gilford progeria syndrome]. | journal=Arch Pediatr | year= 2011 | volume= 18 | issue= 2 | pages= 156-9 | pmid=21251803 | doi=10.1016/j.arcped.2010.11.014 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21251803  }}</ref>
*The [[incidence]] of [[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) in Netherlands is 1:4,000,000.<ref name="pmid168383302">{{cite journal| author=Hennekam RC| title=Hutchinson-Gilford progeria syndrome: review of the phenotype. | journal=Am J Med Genet A | year= 2006 | volume= 140 | issue= 23 | pages= 2603-24 | pmid=16838330 | doi=10.1002/ajmg.a.31346 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16838330  }}</ref>


===Prevalence===
===Prevalence===
*The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
*The [[prevalence]] of [[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) is approximately 1 in 20 million 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===
===Age===
*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===
*[[Hutchinson-Gilford progeria syndrome]] (HGPS) commonly affects individuals of very younger age rather than older age.
*Patients of all age groups may develop [disease name].
*The median age at diagnosis is 2.9 years overall.<ref name="pmid168383304">{{cite journal| author=Hennekam RC| title=Hutchinson-Gilford progeria syndrome: review of the phenotype. | journal=Am J Med Genet A | year= 2006 | volume= 140 | issue= 23 | pages= 2603-24 | pmid=16838330 | doi=10.1002/ajmg.a.31346 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16838330  }}</ref>
*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===
===Race===
*There is no racial predilection to [disease name].
*[Disease name] usually affects individuals of the [race 1] race. [Race 2] individuals are less likely to develop [disease name].
===Gender===
*[Disease name] affects men and women equally.
*[Gender 1] are more commonly affected by [disease name] than [gender 2]. The [gender 1] to [gender 2] ratio is approximately [number > 1] to 1.


===Region===
* [[Hutchinson-Gilford progeria syndrome]] (HGPS) usually affects individuals of the white race.
*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].
===Gender===
 
*[[Hutchinson-Gilford progeria syndrome]] ([[HGPS]]) affects men and women equally but males are little more commonly affected by [[Hutchinson-Gilford progeria syndrome]] than females.
===Developed Countries===
*The male to female ratio is approximately 1.5:1.<ref name="pmid168383303">{{cite journal| author=Hennekam RC| title=Hutchinson-Gilford progeria syndrome: review of the phenotype. | journal=Am J Med Genet A | year= 2006 | volume= 140 | issue= 23 | pages= 2603-24 | pmid=16838330 | doi=10.1002/ajmg.a.31346 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16838330  }}</ref>
 
===Developing Countries===


==References==
==References==

Latest revision as of 15:40, 9 August 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]

Overview

Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare hereditary disease. The incidence of Hutchinson-Gilford progeria syndrome (HGPS) is very rare. The usual age of diagnosis for Hutchinson-Gilford progeria syndrome (HGPS) ia around two to three years of age. Approximately 100 cases of Hutchinson-Gilford progeria syndrome (HGPS) have been reported in the literature till now worldwide.

Epidemiology and Demographics

Incidence

Prevalence

Age

Race

Gender

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. ↑ Doubaj Y, Lamzouri A, Elalaoui SC, Laarabi FZ, Sefiani A (2011). "[Three cases of Hutchinson-Gilford progeria syndrome]". Arch Pediatr. 18 (2): 156–9. doi:10.1016/j.arcped.2010.11.014. PMID 21251803.
  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.
  5. ↑ 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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