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51 Possible Causes for Generalized Dystonia, Myopathy, Subacute Clinical Course

  • Rhabdomyolysis

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

  • Fibromyalgia

    The generalized dystonia was probably due to the patient's analgesic protective attitude. The actual therapy is still based on the biopsychosocial approach.[] Myopathy with Lactic Acidosis, Hereditary Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset Myopathy, Granulovacuolar Lobular, with Electrical Myotonia[] Pain was subacute in onset, chronic in course, neuropathic, nociceptive, regional, or diffuse and sometimes attributed to fibromyalgia (6%) or psychogenic cause (13%).[]

  • Stiff-Person Syndrome

    Initial misdiagnoses included functional movement disorder (n   2), generalized dystonia and parkinsonism (n   1), and hereditary spastic paraparesis (n   1).[] ( 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[] Encephalomyelitis with rigidity follows a relentless subacute course, leading to death within 3 years.[]

  • Myoglobinuria

    We studied an 8-year-old boy of non-Jewish, Mexican-American descent with autosomal-dominant dystonia musculorum deformans who developed rapidly progressive and severe generalized[] We report on a 23-year-old man in whom recurrent myoglobinuria was observed due to necrotizing vacuolar myopathy confirmed on muscle biopsy.[] The clinical course is complicated by advanced liver dysfunction and by severe cardiomyopathy.[]

  • Nemaline Myopathy

    […] bulbospinal muscular atrophy Generalized epilepsy with febrile seizures-plus Generalized epilepsy-paroxysmal dyskinesia syndrome Generalized isolated dystonia Genetic central[] Nemaline myopathy is divided into six types.[] Our experience confirms that SLONM is clinically characterized by subacute proximal and axial muscle weakness.[]

  • Granulomatosis with Polyangiitis

    0001332 Epileptic encephalopathy 0200134 Generalized myoclonic seizures 0002123 Hyperreflexia Increased reflexes 0001347 Hypertonia 0001276 Intellectual disability Mental[] […] junction والعضلات Myasthenia gravis - Muscular dystrophy - Myotonic dystrophy - Myotonia congenita - Thomsen disease - Neuromyotonia - Paramyotonia congenita - Centronuclear myopathy[] Disorder of involuntary muscle movements 0100660 Dysphagia Poor swallowing Swallowing difficulties Swallowing difficulty [ more ] 0002015 Dyspnea Trouble breathing 0002094 Dystonia[]

  • Polyglucosan Body Myopathy Type 2

    , susceptibility to, 12} 614847 138140 Autosomal dominant SLC2A1 1p34.2 Dystonia 9 601042 138140 Autosomal dominant SLC2A1 1p34.2 GLUT1 deficiency syndrome 1, infantile onset[] Glycogenin-1 (GYG1) gene mutations in a family with polyglucosan body myopathy. Neurol Genet. 2015;1(3):e21.[] The clinical course is complicated by advanced liver dysfunction and by severe cardiomyopathy.[]

  • Proximal Myopathy with Extrapyramidal Signs

    […] lipomatosis Leber hereditary optic neuropathy (LHON) Subacute painless b/l visual failure M:F, 4:1 Median age of onset 24 y Dystonia Cardiac preexcitation syndromes Mitochondrial[] MalaCards based summary : Myopathy with Extrapyramidal Signs, is also known as proximal myopathy with extrapyramidal signs , and has symptoms including tremor and involuntary[] The clinical course is complicated by advanced liver dysfunction and by severe cardiomyopathy.[]

  • Botulism

    No general consensus exists among users of BoNT regarding the need for EMG guidance while injecting the compound for cervical dystonia.[] […] the latest anesthetic implications in regards to coexisting diseases, procedures, drugs, and alternative and complementary therapies, including coverage of mitochondrial myopathy[] Neuromuscular Poliomyelitis Infantile spinal muscular atrophy Acute polyneuropathy (Guillain-Barré syndrome) Congenital myasthenia gravis Muscular dystrophy and congenital myopathy[]

  • Isolated Complex I Deficiency

    […] homologue 2) DDP and OPA1 are involved in MNGIE, Leigh syndrome, cardioencephalomyopathy, deafness-dystonia syndrome and optic atrophy, respectively.[] We present the clinical, biochemical and molecular genetic data in a young girl whose clinical picture is dominated by chronic renal failure, myopathy and persistent lactic[] The course can be acute, subacute, episodic, or chronically progressive. Generally, the later the onset, the slower the progression of the disease.[]

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