SRD5A2 gene mutations--a population-based review

Pediatr Endocrinol Rev. 2010 Sep;8(1):34-40.

Abstract

Knowledge of steroid 5 alpha-reductase type 2 (SRD5A2) gene mutations is expanding, and its role has been implicated in various disease susceptibilities concerning reproductive health. Extensive research has revealed the tendency for specific SRD5A2 gene mutations to be passed along certain racial, ethnic and geographically isolated groups, which suggests population specificity of these mutations. The review provides evidence of variation in the mutational spectrum of the SRD5A2 gene leading to population-specific high prevalence of characteristic disease or phenotypic expression.

Publication types

  • Review

MeSH terms

  • 3-Oxo-5-alpha-Steroid 4-Dehydrogenase / genetics*
  • Alleles
  • Dihydrotestosterone / blood
  • Disorders of Sex Development / enzymology
  • Disorders of Sex Development / genetics
  • Genetic Variation
  • Genitalia, Male / enzymology
  • Humans
  • Hypospadias / enzymology
  • Hypospadias / genetics
  • Male
  • Membrane Proteins / genetics*
  • Mutation*
  • Population Groups / genetics
  • Prostatic Neoplasms / enzymology
  • Prostatic Neoplasms / genetics
  • Testosterone / blood

Substances

  • Membrane Proteins
  • Dihydrotestosterone
  • Testosterone
  • 3-Oxo-5-alpha-Steroid 4-Dehydrogenase
  • SRD5A2 protein, human