Cerebellar hypoplasia-tapetoretinal degeneration syndrome

Orpha code: 2246OMIM code: 213000

Definicja

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
Klasyfikacja

Malformation syndrome

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

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl