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- W2160288088 abstract "Olivopontocerebellar atrophy (OPCA) is rare in childhood and onset in infancy is uncommon. We encountered 11 consecutive children with clinical and radiological features of OPCA which started in infancy. In addition to cerebellar ataxia, these children also had sensorineural deafness and speech impairment. Of the present cases, 8 were sporadic and the pedigree patterns in 3 (with a sibling also involved) point to an AR inheritance. The CT scan showed varying degrees of cerebellar and ppntine atrophy. The underlying genetic and neurochemical substrates of this syndrome await further study." @default.
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- W2160288088 date "2009-01-29" @default.
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- W2160288088 title "A syndrome of olivopontocerebellar atrophy and deafness with onset in infancy" @default.
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- W2160288088 doi "https://doi.org/10.1111/j.1600-0404.1995.tb00419.x" @default.
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