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301 Possible Causes for Lactate Dehydrogenase Increased, Myopathy

  • Glycogen Storage Disease Type 2

    dehydrogenase are increased in most patients with PD but may occasionally be within normal limits in those with adult-onset PD. 34 Muscle biopsies for primary diagnostic[dx.doi.org] At late-onset, the spectrum of vacuolar myopathy is more divergent, ranging from almost normal to severe.[ncbi.nlm.nih.gov] Serum enzymes such as aspartate aminotransferase (AST), alanine aminotransferase (ALT), or lactate dehydrogenase (LDH) may be elevated and may reflect enzymes released from[dx.doi.org]

  • Polymyositis

    KEYWORDS: Branched-chain amino acids; Glucocorticoid; Polymyositis; Steroid myopathy[ncbi.nlm.nih.gov] myopathies.[ncbi.nlm.nih.gov] We herein attempted to determine the features and etiologies of these myopathies.[ncbi.nlm.nih.gov]

  • Dermatomyositis

    The level of similarity between juvenile and adult myopathies regarding the presence of myositis-specific autoantibodies has not been fully elucidated.[ncbi.nlm.nih.gov] BACKGROUND: Dermatomyositis (DM) is inflammatory myopathy or myositis characterized by muscle weakness and skin manifestations.[ncbi.nlm.nih.gov] BACKGROUND: There are scarce studies in the literature about hyaluronic acid in systemic autoimmune myopathies.[ncbi.nlm.nih.gov]

  • Duchenne Muscular Dystrophy

    Occasionally, an increased alanine aminotransferase, aspartate aminotransferase, or lactate dehydrogenase concentration prompts an inappropriate focus on hepatic dysfunction[ncbi.nlm.nih.gov] It is associated with a wide variety of myopathic disorders that affect paraspinal muscles, including inflammatory and inherited myopathies.[ncbi.nlm.nih.gov] MRI, EMG and NCV were compatible with proximal muscle myopathy.[ncbi.nlm.nih.gov]

  • Childhood Dermatomyositis

    Juvenile dermatomyositis, the most common inflammatory myopathy of childhood, is a rare systemic autoimmune vasculopathy that is characterised by weakness in proximal muscles[ncbi.nlm.nih.gov] […] enzyme defect, especially CCO deficiency is present not only in genetic disorders with mitochondrial involvement but in other neuromuscular disorders including inflammatory myopathies[ncbi.nlm.nih.gov] Inflammatory myopathies: Polymyositis, dermatomyositis, and related conditions.[link.springer.com]

  • Rhabdomyolysis

    […] 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] How common is statin induced myopathy?[doi.org]

  • Multiple Myeloma

    Also, reflecting this aggressive clinical presentation, a higher proportion of patients with pPCL have significant leukocytosis, elevated lactate dehydrogenase (LDH) and β2[doi.org] Neurologic findings may include a sensory level change (ie, loss of sensation below a dermatome corresponding to a spinal cord compression), neuropathy, myopathy, a Tinel[emedicine.medscape.com] […] or pain without tenderness Neurologic assessment: Sensory level change (ie, loss of sensation below a dermatome corresponding to a spinal cord compression), neuropathy, myopathy[emedicine.medscape.com]

  • Myotonia Congenita

    Heterozygotes are often asymptomatic but for some mutations heterozygosity is sufficient to cause pronounced myotonia, although without weakness and myopathy.[ncbi.nlm.nih.gov] However, a deficiency of the enzyme has been described in many conditions, including myopathies, neuropathies, and motor neuron disease.[ncbi.nlm.nih.gov] G72.0 Drug-induced myopathy G72.1 Alcoholic myopathy Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.[icd10data.com]

  • Traumatic Rhabdomyolysis

    […] or muscle compression (eg, crush syndrome or prolonged immobilization) -Nontraumatic exertional (eg, marked exertion in untrained individuals, hyperthermia, or metabolic myopathies[forums.acdis.org] It can be induced by numerous factors, including a crush injury to a limb, overuse of skeletal muscle, heat, alcoholism, viral infections, metabolic disorders, myopathies,[nejm.org] .- ) muscular dystrophies and myopathies ( G71 - G72 ) myopathy in amyloidosis ( E85.- ) myopathy in polyarteritis nodosa ( M30.0 ) myopathy in rheumatoid arthritis ( M05.32[icd10data.com]

  • Acute Exertional Rhabdomyolysis

    The rare cases of acute renal failure in marathon runners may be a situation of the ‘perfect storm’ where there are several factors (heat stress, dehydration, latent myopathy[link.springer.com] Minicore (multicore) myopathy Minicore (multicore) myopathy Minicore myopathy, also called, multicore myopathy and multiminicore myopathy, falls under the umbrella of congenital[docplayer.net] Called also azoturia, Monday morning disease, tying up syndrome, capture myopathy. rhabdomyolysis disintegration of striated muscle fibers with excretion of myoglobin in the[medical-dictionary.thefreedictionary.com]

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