Disomy of distal Xq in males: case report and overview

Am J Med Genet A. 2004 Jul 15;128A(2):165-9. doi: 10.1002/ajmg.a.30088.

Abstract

A 46,XYq 8-year-old male was referred for microcephaly, growth, and mental retardation, hypotonia, genital hypoplasia, and dysmorphisms. FISH analysis showed that the rearranged Y chromosome originated from an unbalanced translocation of Xq27.3-qter onto the deleted Yq11.22. Analysis of reported patients with disomy of region distal to Xq26 suggests that this rare anomaly, associated with failure to dosage compensate X-linked genes that are normally inactivated, when present in two copies, is causing a quite distinct phenotype. This imbalance is the aberrant by product of the recombinogenic pairing of the distal pseudoautosomal Xq-Yq region at male meiosis.

Publication types

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

MeSH terms

  • Abnormalities, Multiple / diagnosis
  • Abnormalities, Multiple / genetics*
  • Child
  • Chromosome Banding
  • Chromosomes, Human, X*
  • Chromosomes, Human, Y
  • Facies
  • Gene Duplication
  • Genetic Markers
  • Humans
  • In Situ Hybridization, Fluorescence
  • Intellectual Disability / genetics
  • Male
  • Meiosis
  • Microcephaly / genetics
  • Models, Genetic
  • Muscle Hypotonia / genetics
  • Phenotype
  • Translocation, Genetic
  • Uniparental Disomy
  • Urogenital Abnormalities / genetics

Substances

  • Genetic Markers