A syndrome of epilepsy, dementia, and amelogenesis imperfecta: genetic and clinical features.

A family is described with six members affected by a syndrome of epilepsy, dementia, and amelogenesis imperfecta (Kohlschütter's syndrome). An autosomal recessive pattern of inheritance is established for this disorder.

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Bibliographic Details
Main Authors: Christodoulou, J, Hall, R K, Menahem, S, Hopkins, I J, Rogers, J G
Format: Artigo
Language:Inglês
Published: 1988
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051610/
https://ncbi.nlm.nih.gov/pubmed/3236364
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