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156 Possible Causes for EMG Shows Myopathic Changes, Loss of Ambulation between Third and Sixth Decade, Persistent Notochordal Canal

  • 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]

  • 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: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • 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: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • 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: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • 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: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Muscular Dystrophy-Dystroglycanopathy Type B6

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

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Muscular Dystrophy-Dystroglycanopathy Type B5

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

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • 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: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Danon Disease

    From Wikidata Jump to navigation Jump to search Human disease ANTOPOL DISEASE PSEUDOGLYCOGENOSIS II Glycogenosis due to LAMP-2 deficiency Glycogen Storage Disease Iib Vacuolar cardiomyopathy and myopathy X-linked Lysosomal glycogen storage disease without acid maltase deficiency (formerly) X-linked vacuolar[…][wikidata.org]

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • 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: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal