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Am J Hum Genet. 1994 Feb;54(2):236-43.

Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3.

Author information

1
Human Genetics Unit, University of Edinburgh, Western General Hospital, UK.

Abstract

X-linked hydrocephalus is a well-defined disorder which accounts for > or = 7% of hydrocephalus in males. Pathologically, the condition is characterized by stenosis or obliteration of the aqueduct of Sylvius. Previous genetic linkage studies have suggested the likelihood of genetic homogeneity for this condition, with close linkage to the DXS52 and F8C markers in Xq28. We have investigated a family with typical X-linked aqueductal stenosis, in which no linkage to these markers was present. In this family, close linkage was established to the DXS548 and FRAXA loci in Xq27.3. Our findings demonstrate that X-linked aqueductal stenosis may result from mutations at two different loci on the X chromosome. Caution is indicated in using linkage for the prenatal diagnosis of X-linked hydrocephalus.

PMID:
8304340
PMCID:
PMC1918160
[Indexed for MEDLINE]
Free PMC Article

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