Create issue ticket

110 Possible Causes for Muscle Biopsy Shows Hypoglycosylation of Alpha Dystroglycan, Onset of Symptoms in First or Second Decade of Life

  • Muscular Dystrophy-Dystroglycanopathy Type C14

    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]

  • 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] Muscle biopsy showed a dystrophy with selectively reduced alpha-dystroglycan glycoepitope immunostaining.[ncbi.nlm.nih.gov] Immunoblots revealed hypoglycosylation of alpha-dystroglycan and loss of laminin binding.[ncbi.nlm.nih.gov]

  • 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: Muscle Biopsy Shows Hypoglycosylation of Alpha Dystroglycan
  • 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: Muscle Biopsy Shows Hypoglycosylation of Alpha Dystroglycan
  • Cardiodysrhythmic Potassium-Sensitive Periodic Paralysis

    […] of signs and symptoms typically beginning in the first or second decade of life (Table 1 ).[doi.org] […] variable phenotype of periodic paralysis, cardiac arrhythmia, and distinctive facial and skeletal anomalies. 2, 16 GENERAL CLINICAL PRESENTATION Patients with PP experience an onset[doi.org]

    Missing: Muscle Biopsy Shows Hypoglycosylation of Alpha Dystroglycan
  • Erb 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]

    Missing: Muscle Biopsy Shows Hypoglycosylation of Alpha Dystroglycan
  • Limb-Girdle Muscular Dystrophy Type 1E

    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: Muscle Biopsy Shows Hypoglycosylation of Alpha Dystroglycan
  • 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: Muscle Biopsy Shows Hypoglycosylation of Alpha Dystroglycan
  • 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]

    Missing: Muscle Biopsy Shows Hypoglycosylation of Alpha Dystroglycan
  • Limb-Girdle Muscular Dystrophy Type 2E

    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: Muscle Biopsy Shows Hypoglycosylation of Alpha Dystroglycan

Further symptoms