The clinical significance of pericentric inversion of the human Y chromosome: a rare "third" type of heteromorphism

J Hered. 1982 May-Jun;73(3):236-8. doi: 10.1093/oxfordjournals.jhered.a109627.

Abstract

A 28-year-old normal East Indian was found to have a pericentric inversion of the Y chromosome. After reviewing the literature, it was concluded that an inverted Y chromosome does not impede the production of normal sperm and does not predispose to non-disjunction of other chromosomes in the progeny. Thus, the earlier concept of nondisjunction was rejected, and it is suggested that aberrant cases with aneuploidy and an inverted Y are fortuitous. The pericentric inverted Y is inherited from generation to generation and has no clinical significance. The prevalence of males with pericentric Y inversion in the general population is approximately 1 per 1000. It is suggested that a pericentric inversion of the Y chromosome is a rare chromosomal heteromorphism and should be called type III.

MeSH terms

  • Adult
  • Chromosome Inversion*
  • Down Syndrome / genetics
  • Female
  • Genetic Carrier Screening
  • Humans
  • Male
  • Sex Chromosomes*
  • X Chromosome
  • Y Chromosome*