Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability

Am J Med Genet A. 2009 Mar;149A(3):490-5. doi: 10.1002/ajmg.a.32535.

Abstract

We describe two males with intellectual disability (ID) and facial dysmorphism, both of whom have non-mosaic Y chromosome rearrangements resulting in deletions of large portions of the Y chromosome. Patient A, with ID, mild dysmorphism, speech delay, Duane anomaly of the eye, hypermetropia and conductive hearing loss, had two structurally rearranged Y chromosomes resulting in both p and q arm deletions in addition to a Yp duplication. Patient B, also with speech and language delay, developmental delay and short stature, had an interstitial deletion of Yq11.21-11.23. Array-CGH excluded the presence of additional submicroscopic rearrangements at the 1 Mb resolution level. A review of males with Y chromosome rearrangements and ID was performed. Our study provides a more detailed molecular cytogenetic assessment of Y rearrangements in individuals with ID than has been previously possible, and facilitates assessment and comparison of other individuals with a Y chromosome rearrangement.

Publication types

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

MeSH terms

  • Child
  • Chromosomes, Artificial, Bacterial
  • Chromosomes, Human, Y*
  • Comparative Genomic Hybridization
  • Cytogenetic Analysis*
  • Developmental Disabilities / genetics*
  • Gene Rearrangement*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Language Development Disorders / genetics*
  • Male
  • Young Adult