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196 Possible Causes for Amyotrophic Lateral Sclerosis 1, Myopathy, Rhabdomyolysis

  • Myoglobinuria

    (AR) Amyotrophic lateral sclerosis 1 (SOD1) Amyotrophic lateral sclerosis 2 (ALS2) Primary lateral sclerosis, juvenile (ALS2) Amyotrophic lateral sclerosis 8 (VAPB) Amyotrophic[meduniwien.ac.at] Rhabdomyolysis and Other Causes of Myoglobinuria In this article Pathophysiology Statins and myotoxicity Rhabdomyolysis can be defined as a clinical syndrome associated with[patient.info] We report on a 23-year-old man in whom recurrent myoglobinuria was observed due to necrotizing vacuolar myopathy confirmed on muscle biopsy.[ncbi.nlm.nih.gov]

  • Statin

    Rhabdomyolysis is syndrome characterized by muscle necrosis which causes the release of myoglobin into the bloodstream.[ncbi.nlm.nih.gov] Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis. J Neurol Sci 1998; 156(1): 65–72.[doi.org] KEYWORDS: anti-HMGCR antibody; idiopathic inflammatory myopathy; necrotizing autoimmune myopathy; statin[ncbi.nlm.nih.gov]

  • Myoadenylate Deaminase Deficiency

    Evans , Amyotrophic Lateral Sclerosis-Like Conditions in Possible Association with Cholesterol-Lowering Drugs , Drug Safety , 10.2165/00002018-200932080-00004 , 32 , 8 , ([doi.org] Myoadenylate deaminase deficiency has to be considered as a cause of severe rhabdomyolysis.[ncbi.nlm.nih.gov] Abstract Absence of AMP-deaminase was demonstrated by histochemical and biochemical methods in a muscle biopsy of a 25-year-old woman with facial and limb girdle myopathy.[ncbi.nlm.nih.gov]

  • Autosomal Dominant Myoglobinuria

    (AR) Amyotrophic lateral sclerosis 1 (SOD1) Amyotrophic lateral sclerosis 2 (ALS2) Primary lateral sclerosis, juvenile (ALS2) Amyotrophic lateral sclerosis 8 (VAPB) Amyotrophic[meduniwien.ac.at] , RHABDOMYOLYSIS, rhabdomyolysis, rhabdomyolysis (diagnosis), Rhabdomyolysis [Disease/Finding], Necrosis of skeletal muscle, Skeletal muscle necrosis, Necrosis of skeletal[fpnotebook.com] Elsevier Health Sciences, ٢٣‏/٠٧‏/٢٠١٤ - 14 من الصفحات Congential myopathies, Muscular dystropies, Glycogen storage diseases of muscle, and Idiopathic and Inflammatory myopathies[books.google.com]

  • Genetic Recurrent Myoglobinuria

    Rhabdomyolysis Rhabdomyolysis. Necrotic myofibers.[neuropathology-web.org] MND include 1) primary lateral sclerosis (PLS), 2) primary muscular atrophy (PMA), and 3) amyotrophic lateral sclerosis (ALS).[mayomedicallaboratories.com] Episodes of rhabdomyolysis usually occur when a person with a metabolic myopathy “overdoes it” (sometimes unknowingly).[mda.org]

  • Myopathic Carnitine Deficiency

    Patients are asymptomatic between episodes of rhabdomyolysis. Etiology Several missense mutations in the CPT2 gene result in the myopathic form of CPT II deficiency.[orpha.net] 文献 P.269 掲載の参考文献 1) Ask-Upmark, E: Precipitating factors in the pathogenesis of amyotrophic lateral sclerosis, Acta Med Scand 170: 717, 1961. 1) "Merritt's Textbook of Neurology[molcom.jp] […] congenital myopathies): Nemaline myopathy Central core disease Centronuclear myopathy a.k.a. myotubular myopathy Inflammatory myopathy: Polymyositis Dermatomyositis Inclusion[learningneurology.com]

  • Myopathy, Endocrine

    ., Oxford 1992, p.53), hypokalemic paralysis, myasthenia syndrome, syndrome amyotrophic lateral sclerosis (syndrome ALS), cerebellar ataxia).[scirp.org] Life-threatening cases can cause rhabdomyolysis (acute muscle breakdown).[mda.org] Presentations range anywhere from acute, painful, and necrotic myopathies, as can occur in statin myopathy, to more insidious presentations such as steroid myopathy.[ncbi.nlm.nih.gov]

  • Dementia

    The SAEs considered to be treatment related in the atorvastatin group were hepatitis, acute renal failure/rhabdomyolysis/pancreatitis, abdominal pain/nausea/chest discomfort[doi.org] Abstract Amyotrophic lateral sclerosis/parkinsonism dementia complex (ALS/PDC) is an endemic disease observed in the Kii peninsula, Guam, and Papua.[ncbi.nlm.nih.gov] […] account for the myopathy has also been suggested [ 44 ].[doi.org]

  • Carcinomatous Myopathic Syndrome

    […] phosphokinase test Electromyography Eyelid twitch Hypotonia Muscle aches Muscle atrophy Muscle biopsy Muscle function loss Muscle twitching Myopathic changes Myotonia congenita Rhabdomyolysis[icdlist.com] 2016) : No change 2018 (effective 10/1/2017) : No change 2019 (effective 10/1/2018) : No change ICD-10-CM Codes Adjacent To G13.0 G12.21 Amyotrophic lateral sclerosis G12.22[icd10data.com] Holonyms for carcinomatous myopathy No holonyms found for carcinomatous myopathy. Hyponyms for carcinomatous myopathy No hyponyms found for carcinomatous myopathy.[wordphd.com]

  • Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

    CK was mildly elevated at rest and over 20,000 U/L during her episode of rhabdomyolysis.[pubfacts.com] Superoxide dismutase : Amyotrophic lateral sclerosis 1 (ALS1); MIN:105400. T-plasminogen activator : Familial hyperfibrinolysis; MIN:173370.[changbioscience.com] […] for a rare disease Glycogen storage disease due to phosphoglycerate mutase deficiency Disease definition Muscle phosphoglycerate mutase deficiency (PGAMD) is a metabolic myopathy[orpha.net]

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