Abstract

A family is described in which bilateral perisylvian polymicrogyria was present in 6 members of 3 consecutive generations. Typical anatomic and clinical findings of the syndrome, with a mild phenotype, were present in the 5 affected women from all 3 generations. More severe impairment was observed in the only affected male individual, a boy, in the third generation. Analysis of the pedigree and severity of the phenotype in the affected boy are consistent with transmission of an X-linked dominant trait, although other patterns of inheritance cannot be ruled out with certainty.

Original languageEnglish
Pages (from-to)1910-1913
Number of pages4
JournalNeurology
Volume52
Issue number9
Publication statusPublished - 1999

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ASJC Scopus subject areas

  • Neuroscience(all)

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