XX true hermaphroditism in southern African blacks: exclusion of SRY sequences and uniparental disomy of the X chromosome

Am J Med Genet. 1995 Jan 2;55(1):53-6. doi: 10.1002/ajmg.1320550115.

Abstract

A molecular investigation of 16 Bantu-speaking Black XX true hermaphrodites was undertaken in an attempt to determine the cause of the disorder. Y-specific sequences, including sequences mapping to the sex-determining region of the Y, were shown to be absent from lymphocyte tissue of all 16 patients tested. Y chromosome sequences were also absent from the ovarian and testicular components of both ovotestes of a single XX true hermaphrodite, thus excluding gonadal mosaicism involving Y chromosome sequences. Since there is evidence for Xp genes involved in testis determination/differentiation, uniparental disomy of the X chromosome was investigated in 14 XXTH families. Uniparental disomy was excluded in 12 of the 14 families, and isodisomy was excluded in the remaining two cases.

MeSH terms

  • Africa, Southern
  • Aneuploidy
  • Base Sequence
  • Black People / genetics*
  • DNA Primers
  • Disorders of Sex Development / genetics*
  • Female
  • Humans
  • Male
  • Molecular Sequence Data
  • Nondisjunction, Genetic*
  • Polymorphism, Restriction Fragment Length
  • Sex Determination Analysis
  • X Chromosome*
  • Y Chromosome

Substances

  • DNA Primers