Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12

Eur J Med Genet. 2007 Nov-Dec;50(6):446-54. doi: 10.1016/j.ejmg.2007.07.003. Epub 2007 Aug 6.

Abstract

We report on a patient with mental retardation, seizures and tall stature with advanced bone age in whom a de novo apparently balanced chromosomal rearrangement 46,XX,t(X;9)(q12;p13.3) was identified. Using array CGH on flow-sorted derivative chromosomes (array painting) and subsequent FISH and qPCR analysis, we mapped and sequenced both breakpoints. The Xq12 breakpoint was located within the gene coding for oligophrenin 1 (OPHN1) whereas the 9p13.3 breakpoint was assigned to a non-coding segment within a gene dense region. Disruption of OPHN1 by the Xq12 breakpoint was considered the major cause of the abnormal phenotype observed in the proband.

Publication types

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

MeSH terms

  • Base Sequence
  • Body Height / genetics*
  • Child
  • Chromosome Aberrations*
  • Chromosome Painting
  • Chromosomes, Human, Pair 12 / genetics*
  • Chromosomes, Human, Pair 9 / genetics
  • Cytoskeletal Proteins / genetics*
  • Female
  • GTPase-Activating Proteins / genetics*
  • Humans
  • Karyotyping
  • Mental Retardation, X-Linked / genetics*
  • Mental Retardation, X-Linked / pathology
  • Molecular Sequence Data
  • Nuclear Proteins / genetics*
  • Nucleic Acid Hybridization
  • Seizures / genetics
  • Translocation, Genetic

Substances

  • Cytoskeletal Proteins
  • GTPase-Activating Proteins
  • Nuclear Proteins
  • OPHN1 protein, human