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850 Possible Causes for Generalized Dystonia, Myopathy

  • Writer's Cramp

    Two cases are reported in which simple writer's cramp turned into dystonic writer's cramp without progression to generalized dystonia.[ncbi.nlm.nih.gov] SIGNIFICANCE: Our findings may suggest pathophysiological differences between focal and generalized dystonia, and may also point to an inferior sensitivity of SEPs in detecting[ncbi.nlm.nih.gov] We have noted also the frequent association of other features of segmental and generalized dystonia in patients with dystonic writers' cramp.[academic.oup.com]

  • Meige Syndrome

    Deep brain stimulation of the globus pallidus internus (GPi DBS) is effective in the treatment of primary segmental and generalized dystonia.[ncbi.nlm.nih.gov] Deep brain stimulation for primary generalized dystonia: long-term outcomes. Arch Neurol 2009;66:465–470. 6. Jankovic J.[e-jmd.org] In addition, there are forms of dystonia that may have a genetic cause: DYT1 dystonia is a rare form of dominantly inherited generalized dystonia that can be caused by a mutation[myjourneywithcervicaldystonia.blogspot.com]

  • Adult-Onset Cervical Dystonia Type DYT23

    DYT1 dystonia typically presents as early onset, generalized dystonia, starting in the legs.[neupsykey.com] COL6A1 Bethlem myopathy COL6A2 Bethlem myopathy type 1 COL6A3 Bethlem myopathy type 2 COL12A1 Borjeson-Forssman-Lehmann syndrome PHF6 Brody myopathy ATP2A1 Brunner syndrome[centogene.com] Multifocal dystonia affects many different parts of the body. Generalized dystonia affects most of the body, frequently involving the legs and back.[wikivisually.com]

  • Spasmodic Torticollis

    This form of focal dystonia is unlikely to spread beyond the neck and shoulders or become generalized dystonia.[dystoniacanada.org] Such a type of focal dystonia is quite unlikely to spread outside the shoulders and neck region and become generalized dystonia.[hxbenefit.com] Fahn S. generalized dystonia: Concept and treatment. Clinical Neuropharmacol 1986; 9 (supl 2): 37-48. 4. Marsden C D. The focal dystonias.[svneurologia.org]

  • Oppenheim Disease

    Treatment: Treatment options include botulinum toxin injections for focal symptoms, pharmacological therapy such as anticholinergics for generalized dystonia and surgical[medigoo.com] […] and Turner), nemaline myopathy, and central core disease.[jnnp.bmj.com] Convert to ICD-10-CM : 333.6 converts directly to: 2015/16 ICD-10-CM G24.1 Genetic torsion dystonia Approximate Synonyms Dystonia, generalized Dystonia, idiopathic torsion[icd9data.com]

  • Rhabdomyolysis

    (2) Crush Injury and Trauma In crush injury and other forms of trauma, rhabdomyolysis is generally due to direct muscle injury and ischaemia.[baggas.tripod.com] […] for patients with mitochondrial myopathies. 5 Conclusion Mitochondrial myopathies should be considered in patients presenting with recurrent muscle pain and elevation of[jaoa.org] Zocor Myopathy A number of patients have reported the onset of Zocor myopathy.[drugdangers.com]

  • Familial Visceral Myopathy

    A missense variant (R183W) in non-muscle actin (ACTB, β-actin) has been linked to a combination of malformations, sensory hearing loss, and delayed-onset generalized dystonia[agajournals.wordpress.com] Histological examination of biopsy specimens and molecular analysis show that this patient had both familial visceral myopathy and a mitochondrial myopathy, suggesting that[ncbi.nlm.nih.gov] Familial visceral myopathy is a form of chronic intestinal pseudoobstruction in which fibrosis of the smooth muscle of the alimentary tract causes protean symptoms of disordered[ncbi.nlm.nih.gov]

  • MELAS Syndrome

    ; alternating with ataxia, dystonia, choreoathetosis and spastic paraplegia.[oatext.com] Abstract Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare neurodegenerative disease caused by the decreased ability[ncbi.nlm.nih.gov] MELAS syndrome (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) is one of the classic mitochondrial encephalomyopathies with variable clinical[ncbi.nlm.nih.gov]

  • Muscle Spasm

    Disclaimer The Dystonia Society provides the information on this page as general information only.[dystonia.org.uk] .- ) muscular dystrophies and myopathies ( G71 - G72 ) myopathy in amyloidosis ( E85.- ) myopathy in polyarteritis nodosa ( M30.0 ) myopathy in rheumatoid arthritis ( M05.32[icd10data.com] Hyperthyroidism (associated with myopathy). Lead poisoning . Sarcoidosis . Hyperparathyroidism (hypercalcaemia). Heavy alcohol ingestion and cirrhosis .[patient.info]

  • Stiff-Person Syndrome

    Initial misdiagnoses included functional movement disorder (n   2), generalized dystonia and parkinsonism (n   1), and hereditary spastic paraparesis (n   1).[jamanetwork.com] ( G72.1 ) cramp and spasm ( R25.2 ) drug-induced myopathy ( G72.0 ) myalgia ( M79.1- ) stiff-man syndrome ( G25.82 ) Type 2 Excludes nontraumatic hematoma of muscle ( M79.81[icd10data.com] Prior diagnoses included psychogenic movement disorder (n   2), idiopathic generalized dystonia and parkinsonism (n   1), and hereditary spastic paraparesis (n   1).[jamanetwork.com]

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