| Literature DB >> 6538752 |
R N Schimke, W A Horton, D L Collins, L Therou.
Abstract
We report on 4 boys (3 in one family) who have a remarkably constant syndrome of childhood-onset choreoathetosis with later spasticity, postnatal microcephaly, growth and mental retardation, apparent external ophthalmoplegia and varying degrees of deafness. The pedigrees are consistent with X-linked inheritance. The syndrome is compared and contrasted with others comprising basal ganglion dysfunction in childhood. It is concluded that clinically and genetically the condition is unique.Entities:
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Year: 1984 PMID: 6538752 DOI: 10.1002/ajmg.1320170125
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299