Hereditary elliptocytosis epidemiology and demographics: Difference between revisions
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*Around 90% of those with this disorder are thought to fall into the asymptomatic population. | *Around 90% of those with this disorder are thought to fall into the asymptomatic population. | ||
===Developed Countries=== | ===Incidence in Developed Countries=== | ||
*It is estimated that its incidence is between 3 and 5 per 10,000 in the USA | *It is estimated that its incidence is between 3 and 5 per 10,000 in the USA | ||
===Developing Countries=== | ===Incidence in Developing Countries=== | ||
*Those of African and Mediterranean descent are of higher risk. | *Those of African and Mediterranean descent are of higher risk. | ||
*Some subtypes of hereditary elliptocytosis are significantly more prevalent in regions where [[malaria]] is [[Endemic (epidemiology)|endemic]]. | *Some subtypes of hereditary elliptocytosis are significantly more prevalent in regions where [[malaria]] is [[Endemic (epidemiology)|endemic]]. |
Revision as of 16:32, 21 September 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Epidemiology and Demographics
- The incidence of hereditary elliptocytosis is hard to determine, as many sufferers of the milder forms of the disorder are asymptomatic and their condition never comes to medical attention.
- Around 90% of those with this disorder are thought to fall into the asymptomatic population.
Incidence in Developed Countries
- It is estimated that its incidence is between 3 and 5 per 10,000 in the USA
Incidence in Developing Countries
- Those of African and Mediterranean descent are of higher risk.
- Some subtypes of hereditary elliptocytosis are significantly more prevalent in regions where malaria is endemic.
- For example, in equatorial Africa its incidence approaches 160 per 10,000, and in Malayan natives its incidence is over 15% (1500-2000 per 10,000).
Gender
- Being an almost wholly autosomal dominant disorder, there is no predilection towards either sex in hereditary elliptocytosis.
- The most important exception to this rule of autosomal dominant inheritance is for a subtype of hereditary elliptocytosis called hereditary pyropoikilocytosis (HPP). This condition is autosomal recessive.