8A02.12
Dystonia associated with heredodegenerative disorders
Distonia associada a transtornos heredodegenerativos
CategoryDefinition
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.
Index Terms
Dystonia associated with heredodegenerative disordersDystonia due to autosomal dominant disordersRapid-onset dystonia-parkinsonismDystonia due to dentatorubropallidoluysian atrophyDystonia due to Huntington diseaseDystonia due to autosomal recessive disordersDystonia due to Wilson diseaseDystonia due to Niemann-Pick disease type CDystonia due to other autosomal recessive metabolic disordersDystonia due to GM2 gangliosidosisDystonia due to Metachromatic leukodystrophyDystonia due to homocystinuriaDystonia due to glutaric acidaemiaDystonia due to Hartnup diseaseDystonia due to ataxia-telangiectasiaDystonia in neurodegeneration with brain iron accumulation type 1NBIA 2 PLA2G6 mutationPANK gene mutationDystonia due to Juvenile Parkinson Disease including Parkin mutationProbable autosomal recessive dystoniaProgressive pallidal degenerationDystonia due to X-linked dominant disordersDystonia due to Rett syndromeDystonia due to X-linked recessive disordersDeafness-dystonia optic atrophy syndromeMohr-Tranebjærg syndromeDystonia due to Pelizaeus-Merzbacher diseaseDystonia due to Lesch-Nyhan syndromeDystonia due to mitochondrial cytopathiesDystonia due to Leber's diseaseDystonia due to other mitochondrial cytopathiesDystonia of variable inheritanceDystonia due to Familial basal ganglia calcificationsDystonia due to certain specified inherited disordersDystonia associated with familial basal ganglia calcificationsDystonia due to isolated hereditary vitamin E deficiencyDystonia due to hereditary spastic paraplegiaDystonia 16Infantile dystonia-parkinsonism