Olivopontocerebellar atrophy deafness
Olivopontocerebellar atrophy-deafness syndrome is characterised by infancy-onset olivopontocerebellar atrophy, sensorineural deafness and speech impairment. It has been described in less than 15 children. Most cases were sporadic, but autosomal recessive inheritance was suggested in three cases.
NIH genetic and rare disease info[edit source]
Olivopontocerebellar atrophy deafness is a rare disease.
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