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50 Possible Causes for Limb Dystonia (18, )

  • Progressive Supranuclear Palsy

    We report a 67-year-old man with 4-repeat (4R) tauopathy sharing both features of corticobasal degeneration (CBD) and progressive supranuclear palsy (PSP). Although CBD and PSP have a common pathological feature that 4R tau accumulates in neurons and glia, recent pathological studies have confirmed[…][ncbi.nlm.nih.gov]

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  • Hereditary Hyperekplexia

    Ulna and fibula absence of with severe limb deficiency Cowden syndrome Dystonia 18 Paroxysmal exertion-induced dyskinesia (PED) is a form of paroxysmal dyskinesia (see this[amp.pharm.mssm.edu] Dystonia 10 Dystonia 16 Dystonia 16 (DYT16) is a very rare and newly discovered movement disorder which is characterized by early-onset progressive limb dystonia, laryngeal[amp.pharm.mssm.edu] […] and oromandibular dystonia, and parkinsonism.[amp.pharm.mssm.edu]

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  • Early-Onset Autosomal Dominant Alzheimer Disease

    […] muscular dystrophy type 2P Autosomal recessive spastic paraplegia type 18 Cerebellar ataxia - hypogonadism Charcot-Marie-Tooth disease type 1F Developmental malformations[csbg.cnb.csic.es] - deafness - dystonia Dravet syndrome Early-onset progressive neurodegeneration - blindness - ataxia - spasticity Epilepsy with myoclonic-astatic seizures Familial amyloid[csbg.cnb.csic.es] Autosomal dominant Charcot-Marie-Tooth disease type 2A1 Autosomal dominant Charcot-Marie-Tooth disease type 2E Autosomal dominant macrothrombocytopenia Autosomal recessive limb-girdle[csbg.cnb.csic.es]

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  • Limb-Girdle Muscular Dystrophy Type 2E

    […] muscular dystrophy type 2F; dilated cardiomyopathy-1L AR 4 SGCE 604149 myoclonus-dystonia AD 21 SGCG 608896 limb-girdle muscular dystrophy type 2C AR 18 SMCHD1 614982 Fascioscapulohumeral[centogene.com] […] disproportion; rigid spine syndrome AD, AR 18 SGCA 600119 limb-girdle muscular dystrophy type 2D AR 9 SGCB 600900 limb-girdle muscular dystrophy type 2E AR 8 SGCD 601411 limb-girdle[centogene.com]

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  • Increased Sweating

    […] years and older with lower limb spasticity to treat the abnormal head position and neck pain that happens with cervical dystonia (CD) in people 16 years and older to treat[botoxseveresweating.com] […] in elbow, wrist, finger, and thumb muscles in people 18 years and older with upper limb spasticity to treat increased muscle stiffness in ankle and toe muscles in people 18[botoxseveresweating.com]

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  • Torticollis

    Botulinum toxin therapy for limb dystonias. Neurology. 1992;42:627–30. . CrossRef PubMed Google Scholar 19. Poungvarin N, Viriyavejakul A, Komoltri C.[doi.org] SpringerPlus 5(1):1292–1296 CrossRef PubMed PubMedCentral Google Scholar 18.[doi.org] Comparative study of primary and secondary hemifacial spasm. 2006;63:441–444 Google Scholar 18. Yoshimura DM, Aminoff MJ, Olney RK.[doi.org]

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  • Spinocerebellar Ataxia Type 6

    , slow saccades, limb and truncal ataxia, titubation, hyper-reflexia SARA score 33 9.5 35 18 16 Dystonia Jaw-opening dystonia Blepharospasm, orobuccal dystonia, antecollis[movementdisorders.org] 52 Age at onset of dystonia (years) 25 43 49 26 58 Course of dystonia Slow progression Slow progression Rapid progression Slow progression Steady Current clinical features[movementdisorders.org] Positive Initial symptom Gait instability Cervical dystonia Gait instability, dysarthria Gait instability Gait instability Age at onset of cerebellar signs (years) 18 55 23 18[movementdisorders.org]

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  • Spinocerebellar Ataxia Type 13

    , slow saccades, limb and truncal ataxia, titubation, hyper-reflexia SARA score 33 9.5 35 18 16 Dystonia Jaw-opening dystonia Blepharospasm, orobuccal dystonia, antecollis[movementdisorders.org] 52 Age at onset of dystonia (years) 25 43 49 26 58 Course of dystonia Slow progression Slow progression Rapid progression Slow progression Steady Current clinical features[movementdisorders.org] Positive Initial symptom Gait instability Cervical dystonia Gait instability, dysarthria Gait instability Gait instability Age at onset of cerebellar signs (years) 18 55 23 18[movementdisorders.org]

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  • Hypertrophic Interstitial Neuropathy

    […] reduction defects syndrome Dyssegmental dysplasia, Rolland-Desbuquois type Dyssegmental dysplasia, Silverman-Handmaker type Dysspondyloenchondromatosis Dystonia 12 Dystonia[orpha.net] […] hemimelica Dysplasia of head of femur, Meyer type Dysplastic cortical hyperostosis Dysplastic gangliocytoma of the cerebellum Dysprothrombinemia Dysraphism-cleft lip/palate-limb[orpha.net] 16 Dystonia 18 Dystonia 23 Dystonia 24 Dystonia 25 Dystonia 29 Dystonia-aphonia syndrome Dystonia musculorum deformans Dystonia-parkinsonism-hypermanganesemia syndrome Dystonia-parkinsonism[orpha.net]

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  • Sneddon's Syndrome

    16 Spastic paraplegia 18 Parkinson disease type 9 Cockayne syndrome type I Limb-girdle muscular dystrophy Gaucher disease type 3 SLC35A2-CDG Malignant hyperthermia susceptibility[checkrare.com] […] muscular dystrophy Trigeminal neuralgia Spinocerebellar ataxia autosomal recessive 8 Primary orthostatic tremor Spinocerebellar ataxia 18 Spinocerebellar ataxia 14 GAPO syndrome[checkrare.com] Dopa-responsive dystonia; Segawa syndrome AD Myosin storage myopathy Neurocutaneous melanosis Grubben de Cock Borghgraef syndrome Spinocerebellar ataxia 26 Congenital myasthenic[checkrare.com]

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