A new point mutation of the androgen receptor gene in a patient with partial androgen resistance and severe oligozoospermia

Andrologia. 1999 Jul;31(4):199-201. doi: 10.1046/j.1439-0272.1999.00278.x.

Abstract

Mutations of the androgen receptor gene in genetic males cause a variety of androgen insensitivity syndromes varying from female phenotype through intersexuality to male phenotype with infertility. The identification of a missense mutation in the steroid-binding domain in an infertile male with mild features of androgen insensitivity is reported here.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Androgen-Insensitivity Syndrome / complications
  • Androgen-Insensitivity Syndrome / genetics*
  • Androgen-Insensitivity Syndrome / metabolism*
  • Base Sequence
  • DNA / genetics
  • Exons
  • Female
  • Humans
  • Male
  • Molecular Sequence Data
  • Oligospermia / complications
  • Oligospermia / genetics*
  • Oligospermia / metabolism*
  • Phenotype
  • Point Mutation*
  • Receptors, Androgen / genetics*
  • Trinucleotide Repeats

Substances

  • Receptors, Androgen
  • DNA