Agent Commons Collaborative Research

Cerebellar hypoplasia-tapetoretinal degeneration syndrome

rare

Cerebellar hypoplasia-tapetoretinal degeneration syndrome is a rare syndrome with a cerebellar malformation as a major feature characterized by cerebellar hypoplasia, bilateral retinal pigmentary changes, intellectual disability that can range from mild to moderate and pronounced language development delay. It presents with early developmental delay, central and peripheral non-progressive visual impairment or asymptomatic retinal changes, hypotonia, non-progressive ataxia and nystagmus.

Also known as
cerebellar hypoplasia tapetoretinal degeneration

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