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Results 1 - 8 of 8 for Muscular "dystrophy," "limb-girdle," autosomal dominant 4
  1. Limb-girdle muscular dystrophy 
    ... DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12 MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, ...
    https://medlineplus.gov/.../condition/limb-girdle-muscular-dystrophy - Genetics
  2. SGCD gene 
    ... Klepper J, Straub V. Does delta-sarcoglycan-associated autosomal-dominant ... muscular dystrophy-associated protein diseases. Neurologist. 2010 Nov;16(6): ...
    https://medlineplus.gov/genetics/gene/sgcd - Genetics
  3. LMNA gene 
    ... in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B). Hum Mol Genet. ...
    https://medlineplus.gov/genetics/gene/lmna - Genetics
  4. Isolated hyperCKemia 
    ... cause other caveolinopathies including CAV3-related distal myopathy, limb-girdle muscular dystrophy, ... This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/isolated-hyperckemia - Genetics
  5. CAV3-related distal myopathy 
    ... CAV3 gene mutations can cause other caveolinopathies including limb-girdle muscular dystrophy, ... This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/.../condition/cav3-related-distal-myopathy - Genetics
  6. Oculopharyngeal muscular dystrophy 
    ... as muscle cells. PABPN1 Most cases of oculopharyngeal muscular dystrophy are inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/.../oculopharyngeal-muscular-dystrophy - Genetics
  7. Rippling muscle disease 
    ... Lisanti MP. Caveolinopathies: mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases. Neurology. 2004 Feb 24;62(4):538-43. doi: 10.1212/wnl.62.4. ...
    https://medlineplus.gov/genetics/condition/rippling-muscle-disease - Genetics
  8. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 
    ... degeneration with Paget-like bone disease Multisystem proteinopathy Muscular dystrophy, limb-girdle, with Paget disease of bone Pagetoid amyotrophic lateral ...
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics