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Logo of jmedgeneJournal of Medical GeneticsVisit this articleSubmit a manuscriptReceive email alertsContact usBMJ
J Med Genet. 2000 August; 37(8): 600–602.
PMCID: PMC1734650

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


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.

Keywords: Xp22.3 deletion; X linked mental retardation; X linked ichthyosis; epilepsy; Rudd syndrome

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