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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[] Rhabdomyolysis and Other Causes of Myoglobinuria In this article Pathophysiology Statins and myotoxicity Rhabdomyolysis can be defined as a clinical syndrome associated with[] We report on a 23-year-old man in whom recurrent myoglobinuria was observed due to necrotizing vacuolar myopathy confirmed on muscle biopsy.[]

  • Statin

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

  • 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 , ([] Myoadenylate deaminase deficiency has to be considered as a cause of severe rhabdomyolysis.[] 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.[]

  • 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[] , RHABDOMYOLYSIS, rhabdomyolysis, rhabdomyolysis (diagnosis), Rhabdomyolysis [Disease/Finding], Necrosis of skeletal muscle, Skeletal muscle necrosis, Necrosis of skeletal[] Elsevier Health Sciences, ٢٣‏/٠٧‏/٢٠١٤ - 14 من الصفحات Congential myopathies, Muscular dystropies, Glycogen storage diseases of muscle, and Idiopathic and Inflammatory myopathies[]

  • Genetic Recurrent Myoglobinuria

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

  • 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.[] 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[] […] congenital myopathies): Nemaline myopathy Central core disease Centronuclear myopathy a.k.a. myotubular myopathy Inflammatory myopathy: Polymyositis Dermatomyositis Inclusion[]

  • Myopathy, Endocrine

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

  • Dementia

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

  • 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[] 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[] Holonyms for carcinomatous myopathy No holonyms found for carcinomatous myopathy. Hyponyms for carcinomatous myopathy No hyponyms found for carcinomatous myopathy.[]

  • 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.[] Superoxide dismutase : Amyotrophic lateral sclerosis 1 (ALS1); MIN:105400. T-plasminogen activator : Familial hyperfibrinolysis; MIN:173370.[] […] for a rare disease Glycogen storage disease due to phosphoglycerate mutase deficiency Disease definition Muscle phosphoglycerate mutase deficiency (PGAMD) is a metabolic myopathy[]

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