A clinico-genetic investigation of Leydig cell hypoplasia

Am J Med Genet. 1987 Feb;26(2):337-44. doi: 10.1002/ajmg.1320260212.

Abstract

We report on a kindred including a patient (46,XY) with typical manifestations of Leydig cell hypoplasia who was born to parents who were first cousins. A sister had secondary amenorrhea possibly due to primary ovarian dysfunction. Analysis of six pedigrees fits to a male-limited autosomal recessive pattern of inheritance; its implication for the mutational dynamics in the populations is evaluated.

Publication types

  • Case Reports

MeSH terms

  • Adrenal Glands / physiopathology
  • Adult
  • Disorders of Sex Development / genetics*
  • Disorders of Sex Development / pathology
  • Disorders of Sex Development / physiopathology
  • Female
  • Humans
  • Karyotyping
  • Leydig Cells / pathology*
  • Male
  • Pedigree
  • Testis / physiopathology