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

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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.

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Gohlke, B. C., Haug, K., Fukami, M., Friedl, W., Noeker, M., Rappold, G. A., & Haverkamp, F. (2000). Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy. Journal of Medical Genetics, 37(8), 600–602. https://doi.org/10.1136/jmg.37.8.600

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