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3,185 Possible Causes for Muscular Atrophy, Tertiary Contractions of the Esophagus

  • Myotonic Dystrophy

    Neuromuscular disorders like myotonic dystrophy (dystrophia myotonica or Steinert's disease) and spinal muscular atrophy are associated with perioperative complications related[] New contributions to the theory of muscular atrophy in supranuclear paralysis especially in cerebral hemiplegia (Habilitationsschrift).[] atrophy (most frequently involving the hands, forearms, and face), myotonia, frontal baldness, lenticular opacities, and testicular atrophy.[]

  • Myasthenia Gravis

    There is no muscular atrophy or loss of sensation.[] RESULTS: We describe a girl with MuSK-antibody positive myasthenia gravis who developed a myopathy with severe generalized muscular weakness, muscle atrophy, and myopathic[] Aird RB Muscular atrophies and dystrophies. Baker ABed. Clinical Neurology. Vol 3 New York, NY Hoeber & Harper1955;1498- 1562 Google Scholar 3.[]

  • 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: Tertiary Contractions of the Esophagus
  • 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: Tertiary Contractions of the Esophagus
  • 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: Tertiary Contractions of the Esophagus
  • 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: Tertiary Contractions of the Esophagus
  • 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: Tertiary Contractions of the Esophagus
  • 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[] […] in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts Applies To Duchenne-Aran muscular atrophy Progressive muscular atrophy (pure[]

    Missing: Tertiary Contractions of the Esophagus
  • Motor Neuron Disease

    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.[] atrophies (NMAs) and compared these patterns to mouse models of neurogenic muscular atrophy.[]

    Missing: Tertiary Contractions of the Esophagus
  • 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[] Continued Spinal Muscular Atrophy This is an inherited condition that affects lower motor neurons. A defect in a gene called SMN1 causes spinal muscular atrophy.[] atrophy (PMA) and spinal muscular atrophies (SMAs) Upper and lower motor neurons - ALS ALS is the most common of the MNDs.[]

    Missing: Tertiary Contractions of the Esophagus

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