Cerebellar hypoplasia-tapetoretinal degeneration syndrome

Orpha code: 2246OMIM code: 213000

Definition

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.

Disease data
Classification

Malformation syndrome

ORPHA code
2246
OMIM code
213000
ICD10 code
Q04.3
ICD11 code
LD20.0Y

No additional description.

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