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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1990 Nov;27(11):688–692. doi: 10.1136/jmg.27.11.688

MASA syndrome: new clinical features and linkage analysis using DNA probes.

C Schrander-Stumpel 1, E Legius 1, J P Fryns 1, J J Cassiman 1
PMCID: PMC1017259  PMID: 2277384

Abstract

We describe a two generation family in which two males have the X linked recessive MASA syndrome (mental retardation, aphasia, shuffling gait, and adducted thumbs). A third male in this family died at the age of 15 years from congenital hydrocephalus. In the present family cerebral abnormalities are reported for the first time. Linkage analysis confirms the chromosome localisation at Xq28. A crossover between the coagulation factor VIII locus (F8C) and MASA syndrome, but not with DXS52 and DXS305, locates the gene on the same side of F8C as DXS52 and DXS305. The possible relationship between MASA syndrome and X linked hydrocephalus is discussed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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