| Literature DB >> 8053659 |
Abstract
A family of 5 affected male infants in 2 generations with an X-linked pattern of inheritance is described. All affected infants manifested intractable seizures, severe psychomotor retardation, growth failure, microphallus, and death during infancy. Three of the affected patients had radiological studies that demonstrated findings consistent with pachygyria-agyria and agenesis of the corpus callosum. We believe that this family represents a form of X-linked pachygyria-agyria (lissencephaly) that has not been described previously and suggests a locus for lissencephaly on the X chromosome.Entities:
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Year: 1994 PMID: 8053659 DOI: 10.1002/ana.410360216
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422