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

Bettina Gohlke, K. Haug, Maki Fukami, Waltraut Friedl, Meinolf Noeker, Gudrun Rappold, F. Haverkamp

Journal of Medical Genetics · 2000 · 41 citations · 13 references

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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.

References

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