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163 Possible Causes for EMG Shows Myopathic Changes, Persistent Notochordal Canal, Proximal Muscle Weakness Limb Girdle Distribution

  • Limb-Girdle Muscular Dystrophy Type 2J

    notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] […] syndrome SLC35A1-CDG SLC35A2-CDG SSR4-CDG STT3A-CDG STT3B-CDG SURF1-related Charcot-Marie-Tooth disease type 4 Sacral agenesis-abnormal ossification of the vertebral bodies-persistent[se-atlas.de]

    Missing: Proximal Muscle Weakness Limb Girdle Distribution
  • Limb-Girdle Muscular Dystrophy Type 2B

    EMG showed myopathic changes and skeletal muscle biopsies showed severe myopathic changes with variation of fiber size, fiber splitting, increased connective tissue, and some[checkorphan.org]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Limb-Girdle Muscular Dystrophy Type 2L

    EMG shows myopathic changes.[egl-eurofins.com] Muscle biopsy reveal myopathic or dystrophic changes with variation in fiber size, central nuclei, fiber splitting, degeneration of muscle fibers, and an increase in connective[egl-eurofins.com]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Limb-Girdle Muscular Dystrophy Type 1F

    EMG shows myopathic changes.[egl-eurofins.com] Muscle biopsy reveal myopathic or dystrophic changes with variation in fiber size, central nuclei, fiber splitting, degeneration of muscle fibers, and an increase in connective[egl-eurofins.com]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Distal Myopathy Type 3

    EMG is often normal or nonspecific and muscle biopsy shows only mild nonspecific myopathic changes.[neuroweb.us] The EMG shows a myopathic pattern and the muscle biopsy reveals dystrophic changes without the presence of rimmed vacuoles and absent dysferlin.[ruralneuropractice.com] Thus, a serum CK that is EMG shows myopathic changes: fibrillation potentials, positive waves, and myopathic MUP. Dx : Dystrophin gene is deleted.[sites.google.com]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Muscular Dystrophy-Dystroglycanopathy Type B6

    EMG revealed the myopathic pattern. Muscle biopsy showed dystrophic changes with absent staining for merosin.[pediatricneurosciences.com]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Muscular Dystrophy-Dystroglycanopathy Type B5

    The EMG showed slight myopathic changes with progressive course during the ages.[ijponline.biomedcentral.com]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Autosomal Recessive Centronuclear Myopathy

    Electromyogram (EMG) and nerve conduction studies may show mild signs of axonal peripheral nerve involvement in addition to prominent myopathic changes [ 77, 79 ].[ojrd.biomedcentral.com]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Danon Disease

    Danon disease (or glycogen storage disease Type IIb ) is a metabolic disorder. [1] Danon disease is an X-linked lysosomal and glycogen storage disorder associated with hypertrophic cardiomyopathy, skeletal muscle weakness, and intellectual disability. [2] Symptoms [ edit ] Males In males the symptoms of Danon Disease[…][en.wikipedia.org]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Myopathy and Diabetes mellitus

    Abstract We report the clinical, biochemical, and molecular genetic findings in a family with an unusual mitochondrial disease phenotype harboring a novel mtDNA tRNA glutamic acid mutation at position 14709. The proband and his sister presented with congenital myopathy and mental retardation and subsequently developed[…][ncbi.nlm.nih.gov]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution