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235 Possible Causes for Electromyogram Abnormal, Mutation in the Tripartite Motif Containing Protein 32 Gene

  • Limb-Girdle Muscular Dystrophy

    LGMD2H - The Tripartite-motif-containing gene 32 ( TRIM32 ) gene spans 14kb of genomic sequence at chromosome 9q33.1 and the transcript is composed of 2 exons, with the first[ncbi.nlm.nih.gov] Moreover, a human muscle LIM protein (MLP) mutation (W4R) associated with dilated cardiomyopathy (DCM) results in a marked defect in Telethonin interaction/ localization ([ncbi.nlm.nih.gov]

  • Peripheral Neuropathy

    Overview Peripheral neuropathy, a result of damage to the nerves outside of the brain and spinal cord (peripheral nerves), often causes weakness, numbness and pain, usually in your hands and feet. It can also affect other areas of your body. Your peripheral nervous system sends information from your brain and[…][mayoclinic.org]

    Missing: Mutation in the Tripartite Motif Containing Protein 32 Gene
  • Muscular Dystrophy

    Becker muscular dystrophy is an inherited disorder that involves slowly worsening muscle weakness of the legs and pelvis. Becker muscular dystrophy is very similar to Duchenne muscular dystrophy. The main difference is that it gets worse at a much slower rate and it is less common. The disorder is passed down[…][web.archive.org]

    Missing: Mutation in the Tripartite Motif Containing Protein 32 Gene
  • Duchenne Muscular Dystrophy

    The longer survival of patients with Duchenne muscular dystrophy due to advances in clinical care has increased the incidence of Duchenne muscular dystrophy-associated cardiomyopathy, a nearly consistent feature in the third decade of life. A 26-year-old patient with Duchenne muscular dystrophy experienced[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Tripartite Motif Containing Protein 32 Gene
  • Primary Lateral Sclerosis

    Electromyogram ( EMG ). During an EMG , your doctor inserts a needle electrode through your skin into various muscles.[drugs.com] Electromyogram ( EMG ). During an EMG, your doctor inserts a needle electrode through your skin into various muscles.[drugs.com] Your doctor may also order an MRI to look for other causes of your symptoms, such as structural abnormalities, multiple sclerosis or spinal cord tumors.[drugs.com]

    Missing: Mutation in the Tripartite Motif Containing Protein 32 Gene
  • Bell's Palsy

    Practice Essentials Bell palsy, also termed idiopathic facial paralysis (IFP), is the most common cause of unilateral facial paralysis. It is one of the most common neurologic disorders of the cranial nerves (see the image below). In the great majority of cases, Bell palsy gradually resolves over time, and its cause is[…][emedicine.com]

    Missing: Mutation in the Tripartite Motif Containing Protein 32 Gene
  • Stiff-Person Syndrome

    […] that may be causing pinched nerves an electromyogram, which can help your doctor evaluate how well the muscles and nerves are working an ultrasound, which can help your doctor[healthline.com] She walked with an abnormal “tin solider” gait. Findings on magnetic resonance imaging of her brain and spine as well as electromyograms were normal.[doi.org] , which can help your doctor check for muscle damage and the presence of certain autoimmune disorders that can cause rigidity MRI and CT scans, which can reveal any bone abnormalities[healthline.com]

    Missing: Mutation in the Tripartite Motif Containing Protein 32 Gene
  • Becker Muscular Dystrophy

    […] changes in the structure of the muscle cells Tests that stain the muscle sample can be used to visualize any muscle proteins present Electromyogram (EMG): Another diagnostic[dovemed.com] […] muscle biopsy, a muscle sample from an individual is removed and examined under a microscope This technique can help to distinguish BMD from other diseases by identifying any abnormal[dovemed.com]

    Missing: Mutation in the Tripartite Motif Containing Protein 32 Gene
  • Progressive Muscular Atrophy

    We present the electrophysiologic data at baseline of 37 patients who were included in our prospective study on sporadic adult-onset progressive muscular atrophy (PMA). The aim was to correlate electrophysiological signs of lower motor neuron (LMN) loss with clinical signs of LMN loss, and to determine the[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Tripartite Motif Containing Protein 32 Gene
  • Secondary Myopathy

    Although changes seen on electromyography are not pathognomonic for any specific disease process, an abnormal electromyogram can indicate if a neuropathy or neuromuscular[aafp.org] electromyograms, evocative muscle biopsy and an abnormal signal on muscle magnetic resonance imaging.[err.ersjournals.com] View/Print Table TABLE 4 Selected Causes of Primary Muscle Weakness Cause Weakness Age of onset/diagnosis Systemic symptoms and findings Laboratory abnormalities Creatine[aafp.org]

    Missing: Mutation in the Tripartite Motif Containing Protein 32 Gene

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