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125 Possible Causes for MRI Shows Increased Connective Tissue and Fat, Onset of Symptoms in First or Second Decade of Life, Skeletal Muscle Biopsy Shows Dystrophic Changes

  • 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]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy

    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] Histopathology of skeletal muscles biopsies showed typical dystrophic changes with many rimmed vacuoles.[ncbi.nlm.nih.gov] Both patients developed a progressive wasting and weakness of limb-girdle muscles in the late forties or early fifties; their facial, ocular, bulbar, and cardiac muscles were[ncbi.nlm.nih.gov]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Congenital Muscular Dystrophy

    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] Pathological analysis of biopsied skeletal muscle showed dystrophic changes with proliferated fibrotic tissue elements as the predominant finding.[ncbi.nlm.nih.gov] . • Skeletal muscle biopsy shows dystrophic change and additional immunohistochemical abnormalities of variable specificity.[medlink.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] . • Skeletal muscle biopsy shows dystrophic change and additional immunohistochemical abnormalities of variable specificity.[medlink.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Congenital Muscular Dystrophy Type 1A

    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] . • Skeletal muscle biopsy shows dystrophic change and additional immunohistochemical abnormalities of variable specificity.[medlink.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Primary Hypergonadotropic Hypogonadism-Partial Alopecia Syndrome

    Characterized by slowly progressive skeletal muscle weakness of the hip and shoulder girdles. Muscle biopsy shows mild dystrophic changes.[ab-y-ss.com] LGMD1B is characterized by slowly progressive skeletal muscle weakness of the hip and shoulder girdles. Muscle biopsy shows mild dystrophic changes.[genscript.com] Characterized by slowly progressive skeletal muscle weakness of the hip and shoulder girdles. Muscle biopsy shows mild dystrophic changes..[antibodyplus.com]

    Missing: MRI Shows Increased Connective Tissue and Fat Onset of Symptoms in First or Second Decade of Life
  • ACE Inhibitor-Induced Angioedema

    The onset of symptoms of HAE tends to occur in the first or second decade of life, with 75% of the patients experiencing their first attack before the age of 15.[academic.oup.com]

    Missing: MRI Shows Increased Connective Tissue and Fat Skeletal Muscle Biopsy Shows Dystrophic Changes
  • Congenital Muscular Dystrophy with Integrin Alpha-7 Deficiency

    . • Skeletal muscle biopsy shows dystrophic change and additional immunohistochemical abnormalities of variable specificity.[medlink.com]

    Missing: MRI Shows Increased Connective Tissue and Fat Onset of Symptoms in First or Second Decade of Life
  • Young Adult-Onset Distal Hereditary Motor Neuropathy

    Age of onset is in the second and third decades of life and rarely in the first. Recovery is usually complete and begins weeks to months after the onset of symptoms.[emedicine.medscape.com]

    Missing: MRI Shows Increased Connective Tissue and Fat Skeletal Muscle Biopsy Shows Dystrophic Changes
  • Limb-Girdle Muscular Dystrophy Type 1H

    LGMD1B is characterized by slowly progressive skeletal muscle weakness of the hip and shoulder girdles. Muscle biopsy shows mild dystrophic changes.[abcam.com]

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