11β-hydroxylase deficiency epidemiology and demographics
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Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
Epidemiology and Demographics
Prevalence
The prevalence of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency in United States is approximately 1 per 100,000 individuals.
Incidence
CAH due to 11-beta-hydroxylase deficiency accounts for 5 to 8 percent of all cases of congenital adrenal hyperplasia. It is estimated that CAH due to 11-beta-hydroxylase deficiency occurs in 1 in 100,000 to 200,000 newborns. This condition is more common in Moroccan Jews living in Israel, occurring in approximately 1 in 5,000 to 7,000 newborns
Case Fatality Rate
Age
Gender
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency affects male and female equally.
Race
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency usually affects individuals of the Jewish race.