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3,103 Possible Causes for EMG Shows Evidence of Reinnervation, Muscular Atrophy

  • Motor Neuron Disease

    For patients with MND affecting the LMNs, the EMG will show evidence of: (1) acute denervation, which is ongoing as motor neurons degenerate, and (2) chronic denervation and[] Some MNDs, such as ALS and some forms of spinal muscular atrophy, are fatal.[] A somewhat better prognosis is seen in progressive muscular atrophy, where patients live up to 25 years.[]

  • Postpoliomyelitis Syndrome

    Laboratory tests are used to show evidence of prior polio and to exclude other diseases: electromyography (EMG) displays signs of reinnervation and denervation both in symptomatic[] atrophy, and poliomyelitis.[] The rate of progression of post-poliomyelitis muscular atrophy is quite variable.[]

  • Peripheral Neuropathy

    Muscular atrophy of hand muscles persisted. Large fibers were involved more extensively than small fibers.[] Boulis works on novel treatments for several nerve disorders, including Amyotrophic Lateral Sclerosis (ALS, also known as Lou Gehrig's disease) and Spinal Muscular Atrophy[]

    Missing: EMG Shows Evidence of Reinnervation
  • Polyneuropathy

    Neuronal Peroneal Muscular Atrophy (HMSN II) Autosomal dominant inheritance is also the case with HMSN II.[] Ciliary neurotrophic factor-induced sprouting preserves motor function in a mouse model of mild spinal muscular atrophy. Hum. Mol.[] Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography .[]

    Missing: EMG Shows Evidence of Reinnervation
  • Carpal Tunnel Syndrome

    Motor complaints relate to thenar muscular weakness and atrophy.[] (particularly peroneal muscular atrophy) resulting in foot dorsiflexor weakness, foot drop, and secondary steppage gait.[] Charcot–Marie–Tooth disease is highly variable in presentation but is characterized by distal symmetric polyneuropathy, 9 with slowly progressive distal muscle weakness and atrophy[]

    Missing: EMG Shows Evidence of Reinnervation
  • Muscular Dystrophy

    Distal muscular dystrophies are a group of inherited primary muscle disorders showing progressive weakness and atrophy preferentially in the hands, forearm, lower legs, or[] muscular dystrophy Spinal muscular atrophy (SMA) Myotonia congenita Myotonic dystrophy Charcot Marie Tooth disease (hereditary sensory motor neuropathy) At the Pediatric[] […] with: Friedreich's ataxia Myasthenia gravis Spinal muscular atrophy Appointments and Location (804) 828-CHOR (2467) Children's Pavilion - Level 3, Pod B ›› Meet the Team[]

    Missing: EMG Shows Evidence of Reinnervation
  • Primary Progressive Multiple Sclerosis

    In late-stage Roche, they have treatments that are being tested for Alzheimer’s disease, Autism, and for Spinal Muscular Atrophy.[] Roche has more than a dozen investigational medicines in clinical development for diseases that include multiple sclerosis, Alzheimer’s disease, spinal muscular atrophy, Parkinson[] 脊髄性筋萎縮症 Spinal muscular atrophy, SMA Type I 脊髄性筋萎縮症(SMA Type I) 1 HPS0158 HPS0159 Spinal muscular atrophy, SMA Type II 脊髄性筋萎縮症(SMA Type II) 1 不要 有 HPS1391 HPS1392 HPS1393[]

    Missing: EMG Shows Evidence of Reinnervation
  • Progressive Muscular Atrophy

    The name "spinal muscular atrophy" is ambiguous as it refers to any of various spinal muscular atrophies, including the autosomal recessive spinal muscular atrophy caused[] KEYWORDS: Lower motor neuron syndrome; Lower motor neuron-onset ALS; PMA; Progressive muscular atrophy[] Our electrophysiological data in patients recently diagnosed with sporadic progressive muscular atrophy are consistent with widespread LMN loss.[]

    Missing: EMG Shows Evidence of Reinnervation
  • Primary Lateral Sclerosis

    This locus had not been implicated in ALS or in hereditary spastic parapareses, spinal muscular atrophy, or spinal and bulbar muscular atrophy. [7] A genetically mediated[] atrophy (PMA) and spinal muscular atrophies (SMAs) Upper and lower motor neurons - ALS ALS is the most common of the MNDs.[] The traditional classification of MNDs is according to the affected cell types, as follows: Upper motor neurons alone - PLS Lower motor neurons alone - Progressive muscular[]

    Missing: EMG Shows Evidence of Reinnervation
  • Amyotrophic Lateral Sclerosis

    The patients were a 54-year-old man with progressive muscular atrophy who underwent removal of internal fixators in the arm and leg, and a 66-year-old woman with amyotrophic[] BACKGROUND: Informal caregivers of patients with Amyotrophic Lateral Sclerosis (ALS) or Progressive Muscular Atrophy (PMA) face stressful demands due to severe impairments[] Excluding lower motor neuron FA and FL cases, progressive muscular atrophy comprised 4% of the sample and had a prognosis similar to typical limb onset ALS.[]

    Missing: EMG Shows Evidence of Reinnervation

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