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Dentatorubral pallidoluysian atrophy

Disease Export to PDF
Name:
Dentatorubral pallidoluysian atrophy
Description:
A rare subtype of autosomal dominant cerebellar ataxia type I characterized by involuntary movements, ataxia, epilepsy, mental disorders, cognitive decline and prominent anticipation.
ORPHAcode:
101
Synonyms:
DRPLA
Dentatorubropallidoluysian atrophy
Naito-Oyanagi disease
XREF(s):
Orphanet
OMIM
ICD-10
Analyte(s):
ATN1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14