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182 Possible Causes for EMG Shows Myopathic Changes, MRI Shows Increased Connective Tissue and Fat, Onset of Symptoms in First or Second Decade of Life

  • Limb-Girdle Muscular Dystrophy Type 2L

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] 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]

  • Limb-Girdle Muscular Dystrophy Type 2B

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] 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: MRI Shows Increased Connective Tissue and Fat
  • Distal Myopathy Type 3

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] EMG is often normal or nonspecific and muscle biopsy shows only mild nonspecific myopathic changes.[neuroweb.us] Childhood onset weakness, contractures, and early cardiac involvement. Symptoms usually develop in the first or second decade of life.[sites.google.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Limb-Girdle Muscular Dystrophy Type 2J

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Muscular Dystrophy-Dystroglycanopathy Type B6

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] EMG revealed the myopathic pattern. Muscle biopsy showed dystrophic changes with absent staining for merosin.[pediatricneurosciences.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • 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: MRI Shows Increased Connective Tissue and Fat Onset of Symptoms in First or Second Decade of Life
  • Muscular Dystrophy-Dystroglycanopathy Type B5

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

    Missing: MRI Shows Increased Connective Tissue and Fat Onset of Symptoms in First or Second Decade of Life
  • 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: MRI Shows Increased Connective Tissue and Fat Onset of Symptoms in First or Second Decade of Life
  • 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: MRI Shows Increased Connective Tissue and Fat Onset of Symptoms in First or Second Decade of Life
  • 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: MRI Shows Increased Connective Tissue and Fat Onset of Symptoms in First or Second Decade of Life