Andersen-Tawil syndrome epidemiology and demographics: Difference between revisions
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{{Andersen-Tawil syndrome}} | {{Andersen-Tawil syndrome}} | ||
{{CMG}}; {{AE}} | {{CMG}}; {{AE}} {{VKG}} | ||
==Overview== | ==Overview== | ||
Andersen-Tawil syndrome is a rare hereditary multisystem disorder transmitted in autosomal dominant pattern. Only 200 cases of Andersen-Tawil syndrome were reported worldwide. | [[Andersen-Tawil syndrome]] is a rare [[hereditary]] multisystem disorder transmitted in [[autosomal dominant]] pattern. Only 200 cases of [[Andersen-Tawil syndrome]] were reported worldwide. | ||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
===Incidence=== | ===Incidence=== | ||
*The incidence of Andersen-Tawil syndrome is approximately less than 1 per 100,000 individuals worldwide.<ref name="NguyenPieper2013">{{cite journal|last1=Nguyen|first1=Hoai-Linh|last2=Pieper|first2=Gerard H.|last3=Wilders|first3=Ronald|title=Andersen–Tawil syndrome: Clinical and molecular aspects|journal=International Journal of Cardiology|volume=170|issue=1|year=2013|pages=1–16|issn=01675273|doi=10.1016/j.ijcard.2013.10.010}}</ref> | *The [[incidence]] of [[Andersen-Tawil syndrome]] is approximately less than 1 per 100,000 individuals worldwide.<ref name="NguyenPieper2013">{{cite journal|last1=Nguyen|first1=Hoai-Linh|last2=Pieper|first2=Gerard H.|last3=Wilders|first3=Ronald|title=Andersen–Tawil syndrome: Clinical and molecular aspects|journal=International Journal of Cardiology|volume=170|issue=1|year=2013|pages=1–16|issn=01675273|doi=10.1016/j.ijcard.2013.10.010}}</ref> | ||
*Only 200 cases of Andersen-Tawil syndrome were reported worldwide. | *Only 200 cases of [[Andersen-Tawil syndrome]] were reported worldwide. | ||
*Patients who are suffering with periodic paralysis Andersen-Tawil syndrome only accounts for less than 10% of these patients | *Patients who are suffering with [[periodic paralysis]] [[Andersen-Tawil syndrome]] only accounts for less than 10% of these patients. | ||
===Prevalence=== | ===Prevalence=== | ||
*The prevalence of Andersen-Tawil syndrome is unknown. | *The exact [[prevalence]] of [[Andersen-Tawil syndrome]] is unknown. | ||
*The prevalence of congenital Long QT syndrome(LQTS) is around 1 in 2000 births. | *The [[prevalence]] of [[congenital]] [[Long QT syndrome]]([[Long QT syndrome|LQTS]]) is around 1 in 2000 births.<ref name="pmid19841298">{{cite journal| author=Schwartz PJ, Stramba-Badiale M, Crotti L, Pedrazzini M, Besana A, Bosi G et al.| title=Prevalence of the congenital long-QT syndrome. | journal=Circulation | year= 2009 | volume= 120 | issue= 18 | pages= 1761-7 | pmid=19841298 | doi=10.1161/CIRCULATIONAHA.109.863209 | pmc=2784143 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19841298 }}</ref> | ||
=== | ===Age=== | ||
*[[Andersen-Tawil syndrome]] commonly affects individuals of younger age, most commonly in the first decade of life younger than 10 years. | |||
* | |||
===Race=== | ===Race=== | ||
*There is no racial predilection to Andersen-Tawil syndrome as of now. | *There is no racial predilection to [[Andersen-Tawil syndrome]] as of now. | ||
===Gender=== | ===Gender=== | ||
*Andersen-Tawil syndrome affects men and women equally | *[[Andersen-Tawil syndrome]] affects men and women equally. | ||
==References== | ==References== | ||
Latest revision as of 23:09, 17 February 2020
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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
Andersen-Tawil syndrome is a rare hereditary multisystem disorder transmitted in autosomal dominant pattern. Only 200 cases of Andersen-Tawil syndrome were reported worldwide.
Epidemiology and Demographics
Incidence
- The incidence of Andersen-Tawil syndrome is approximately less than 1 per 100,000 individuals worldwide.[1]
- Only 200 cases of Andersen-Tawil syndrome were reported worldwide.
- Patients who are suffering with periodic paralysis Andersen-Tawil syndrome only accounts for less than 10% of these patients.
Prevalence
- The exact prevalence of Andersen-Tawil syndrome is unknown.
- The prevalence of congenital Long QT syndrome(LQTS) is around 1 in 2000 births.[2]
Age
- Andersen-Tawil syndrome commonly affects individuals of younger age, most commonly in the first decade of life younger than 10 years.
Race
- There is no racial predilection to Andersen-Tawil syndrome as of now.
Gender
- Andersen-Tawil syndrome affects men and women equally.
References
- ↑ Nguyen, Hoai-Linh; Pieper, Gerard H.; Wilders, Ronald (2013). "Andersen–Tawil syndrome: Clinical and molecular aspects". International Journal of Cardiology. 170 (1): 1–16. doi:10.1016/j.ijcard.2013.10.010. ISSN 0167-5273.
- ↑ Schwartz PJ, Stramba-Badiale M, Crotti L, Pedrazzini M, Besana A, Bosi G; et al. (2009). "Prevalence of the congenital long-QT syndrome". Circulation. 120 (18): 1761–7. doi:10.1161/CIRCULATIONAHA.109.863209. PMC 2784143. PMID 19841298.