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1,619 Possible Causes for EMG Shows Evidence of Reinnervation, Lactate Dehydrogenase Increased, Muscle Biopsy Abnormal

  • 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] Diagnosis of Duchenne Muscular Dystrophy A muscle biopsy (taking a sample of muscle) for dystrophin studies can be done to look for abnormal levels of dystrophin in the muscle[disabled-world.com] […] fibers) For Duchenne and Becker muscular dystrophies, muscle biopsy may show whether dystrophin, a muscle protein, is missing or abnormal, and DNA testing is used to analyze[webmd.com]

    Missing: EMG Shows Evidence of Reinnervation
  • Amyotrophic Lateral Sclerosis

    For example, NSC-34 cells treated with CSF from patients with ALS exhibited decreased cell viability and increased lactate dehydrogenase activity [ 48 ], suggesting that factors[doi.org] Only about 10% of ALS patients have abnormal nerve conduction study results, but the test can also suggest other diagnoses. A muscle biopsy.[webmd.com] Further analyses in the same study also showed that Chit-1 increased expression in microglia upon exposure to CSF from patients with ALS, suggesting its role in microglial[doi.org]

    Missing: EMG Shows Evidence of Reinnervation
  • Polymyositis

    dehydrogenase [ LDH ], aldolase, myoglobin), hypergammaglobulinemia, increased erythrocyte sedimentation rate ( ESR ) and C-reactive protein ( CRP ) levels. 2) Immunologic[empendium.com] Muscle biopsy abnormalities at some time during their disease: i. degeneration and regeneration of muscle fibers ii. necrosis iii. phagocytosis iv. interstitial mononuclear[clinicaltrials.gov] Laboratory testing showed elevated muscle enzymes and myopathic abnormalities on electromyographic examination.[ncbi.nlm.nih.gov]

    Missing: EMG Shows Evidence of Reinnervation
  • Myopathy

    The laboratory evaluation was remarkable for the marked increase in the serum lactate dehydrogenase and creatine phosphokinase levels.[ncbi.nlm.nih.gov] Clinical presentation, abnormal secretion of the collagen demonstrated in muscle biopsy and the COL6A1 c.1056 3A C mutation justify classification of the presented case as[ncbi.nlm.nih.gov] Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy. J Neurol Neurosurg Psychiatry. 2006;77:208-15.[rarediseases.org]

    Missing: EMG Shows Evidence of Reinnervation
  • 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] A muscle tissue biopsy may be assayed for muscle glycogen phosphorylase enzyme activity.[encyclopedia.com] […] in muscle Heterozygotes: Manifesting patients described Variant syndrome Symptoms associated with statin use: 1 patient Lactate dehydrogenase A deficiency (GSD 11) L-lactate[neuromuscular.wustl.edu]

    Missing: EMG Shows Evidence of Reinnervation
  • Dermatomyositis

    Muscle biopsy abnormalities at some time during their disease: i. degeneration and regeneration of muscle fibers ii. necrosis iii. phagocytosis iv. interstitial mononuclear[clinicaltrials.gov] Muscle biopsy abnormalities at some time during their disease: Muscle fiber destruction; Muscle fiber regeneration; Perivascular and interstitial inflammatory infiltrates[clinicaltrials.gov] EMG characteristic muscle biopsy abnormalities and absence of histopathologic signs of other myopathies Signs and Symptoms Grotton’s Sign: An erythematous, scaly eruption[docsity.com]

    Missing: EMG Shows Evidence of Reinnervation
  • Childhood Dermatomyositis

    The subsequent list, derived from the first survey, comprised MRI abnormalities suggestive of inflammatory myositis; calcinosis; changes on muscle biopsy typical of myositis[rheumatology.oxfordjournals.org] […] weakness, raised serum muscle enzymes, electromyographic abnormalities and consistent muscle biopsy findings .[indianpediatrics.net] Changes on muscle biopsy typical of myositis 61.3 87.4 Abnormalities on MRI suggestive of inflammatory myositis 58 70.6 Other: factor VIII-related (von Willebrand) antigen[rheumatology.oxfordjournals.org]

    Missing: EMG Shows Evidence of Reinnervation
  • Myotonia Congenita

    Biopsied muscle specimens and EMG findings showed non-specific mild myopathic changes. There was no abnormal expansion of CTG repeat within the myotonic dystrophy gene.[ncbi.nlm.nih.gov] We have investigated the muscle biopsies of 8 patients with myotonia congenita.[ncbi.nlm.nih.gov] Electromyographic examinations disclosed myotonic discharge with dive bomber sounds at insertion, and high-amplitude, high-frequency motor unit potentials during the muscle[ncbi.nlm.nih.gov]

    Missing: EMG Shows Evidence of Reinnervation
  • Trichinellosis

    Other blood tests that are elevated, but not specific for trichinosis, are creatine kinase, and lactate dehydrogenase (enzymes that increase in the blood when muscle cells[medicinenet.com] Table 2 Laboratory findings in human trichinellosis Muscle enzymes such as creatine phosphokinase (CPK) and lactate dehydrogenase (LDH) may remain raised for more than four[doi.org] An increased CPK isoenzyme-MB level, generally ascribed to myocardial damage, has been observed in 35% of trichinellosis patients examined, with no cardiological symptons,[doi.org]

    Missing: EMG Shows Evidence of Reinnervation
  • Contusion

    Biopsy was deferred. One month later, the imaging abnormality had nearly disappeared.[ncbi.nlm.nih.gov] In retrospect, it represented a contusion injury of the longus colli muscle, a finding not reported previously.[ncbi.nlm.nih.gov]

    Missing: EMG Shows Evidence of Reinnervation