Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy

J Med Genet. 2000 Aug;37(8):600-2. doi: 10.1136/jmg.37.8.600.

Abstract

We describe monozygotic male twins with an interstitial deletion of Xp22.3 including the steroid sulphatase gene (STS). The twins had X linked ichthyosis, X linked mental retardation, and epilepsy. A locus for X linked mental retardation has been assigned to a region between STS and DXS31 spanning approximately 3 Mb. Recently the locus was further refined to an approximately 1 Mb region between DXS1060 and GS1. By PCR analysis of flanking STS gene markers in our patients we succeeded in narrowing down the locus to between DXS6837 and GS1.

Publication types

  • Case Reports

MeSH terms

  • Arylsulfatases / genetics*
  • Child
  • Epilepsy / etiology
  • Epilepsy / genetics*
  • Gene Deletion*
  • Genetic Linkage
  • Humans
  • Ichthyosis / etiology
  • Ichthyosis / genetics*
  • Infant
  • Intellectual Disability / etiology
  • Intellectual Disability / genetics*
  • Male
  • Steryl-Sulfatase
  • Twins
  • X Chromosome / genetics*

Substances

  • Arylsulfatases
  • Steryl-Sulfatase