| Literature DB >> 3239950 |
D N Black1, G V Watters, E Andermann, C Dumont, M E Kabay, P Kaplan, K Meagher-Villemure, J Michaud, G O'Gorman, E Reece.
Abstract
We report a neurological disease among Cree Indian children in a northern Quebec village. The disease manifests as severe mental retardation, cerebral atrophy with white matter changes and calcifications, and systemic immunological abnormalities. Eleven cases are known in five families. The familial incidence of cases and the high degree of parental consanguinity suggest a genetic contribution. We propose that this entity may be caused by an unusual viral infection in a genetically vulnerable host.Entities:
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Year: 1988 PMID: 3239950 DOI: 10.1002/ana.410240402
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422