Max Planck Institute for Molecular Genetics

Max Planck Institute for Molecular Genetics - Ihnestraße 63-73 - 14195 Berlin - Germany - Phone: (+49 30) 8413 0 - Fax: (+49 30) 8413 1394
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 [back to Human Molecular Genetics]Human Molecular Genetics Research Group Familial Cognitive Disorders


X-linked mental retardation

Autosomal recessive mental retrardation

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  German Mental Retardation Network (MRNET)

X-Linked Mental Retardation

X-linked pedigree
Mental retardation (MR) affects approximately 30% more males than females. This is partly due to the X-chromosomal location of relevant genetic defects, and recent years have seen important progress in the identification of the genes involved in X-linked mental retardation (XLMR). Two main forms of XLMR - syndromic XLMR (S-XLMR), which is associated with additional phenotypes, and non-syndromic XLMR (NS-XLMR) - are being distinguished with NS-XLMR being the more common form, affecting 2/3 of the patients. However, while the majority of the genetic defects that underlie S-XLMR is either known or has been mapped to small chromosomal regions, less than 50% of those that underlie NS-XLMR have been identified (For Review see e.g. Ropers 2008, Ropers 2007, Ropers & Hamel 2005)

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