Periventricular heterotopia and epilepsy
- PMID: 8290091
- DOI: 10.1212/wnl.44.1.51
Periventricular heterotopia and epilepsy
Abstract
We report a family with nodular subependymal masses of heterotopic gray matter occurring in six members in four generations. Only female members of the family are affected, and there is a high rate of spontaneous abortion, consistent with X-linked dominant inheritance, and lack of viability in affected males. Both in this family and in sporadic cases of subependymal heterotopias there is a high frequency of convulsive disorders, suggesting that epilepsy may be the major clinical manifestation of this developmental defect.
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