Olivopontocerebellar atrophy-deafness syndrome

Olivopontocerebellar atrophy-deafness syndrome is characterized 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.

Also known as: olivopontocerebellar atrophy deafness

0 clinical trials for this condition and its sub-types, 0 tagged with Olivopontocerebellar atrophy-deafness syndrome itself.