8A02.12
category
Dystonia associated with heredodegenerative disorders
Definition
Dystonia occurring as a part of a more complex heredodegenerative disorder. It is not a pure dystonia and other neurological findings such as ataxia, pyramidal signs and cognitive issues may be seen.
Also indexed as
Deafness-dystonia optic atrophy syndromeDystonia 16Dystonia associated with familial basal ganglia calcificationsDystonia associated with heredodegenerative disordersDystonia due to Familial basal ganglia calcificationsDystonia due to GM2 gangliosidosisDystonia due to Hartnup diseaseDystonia due to Huntington diseaseDystonia due to Juvenile Parkinson Disease including Parkin mutationDystonia due to Leber's diseaseDystonia due to Lesch-Nyhan syndromeDystonia due to Metachromatic leukodystrophyDystonia due to Niemann-Pick disease type CDystonia due to Pelizaeus-Merzbacher diseaseDystonia due to Rett syndromeDystonia due to Wilson diseaseDystonia due to X-linked dominant disordersDystonia due to X-linked recessive disordersDystonia due to ataxia-telangiectasiaDystonia due to autosomal dominant disordersDystonia due to autosomal recessive disordersDystonia due to certain specified inherited disordersDystonia due to dentatorubropallidoluysian atrophyDystonia due to glutaric acidaemiaDystonia due to hereditary spastic paraplegiaDystonia due to homocystinuriaDystonia due to isolated hereditary vitamin E deficiencyDystonia due to mitochondrial cytopathiesDystonia due to other autosomal recessive metabolic disordersDystonia due to other mitochondrial cytopathiesDystonia in neurodegeneration with brain iron accumulation type 1Dystonia of variable inheritanceInfantile dystonia-parkinsonismMohr-Tranebjærg syndromeProbable autosomal recessive dystoniaProgressive pallidal degenerationRapid-onset dystonia-parkinsonism