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Results 1 - 10 of 15 for Autosomal recessive "limb-girdle" muscular dystrophy
  1. ... individuals eventually require wheelchair assistance. DYSF_HUMAN dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive) dystrophy-associated fer-1-like 1 fer-1- ...
  2. ... the disorder that have an inheritance pattern called autosomal recessive.Calpainopathy, or limb-girdle muscular dystrophy type 2A, is caused by mutations in the ...
  3. Limb-Girdle Muscular Dystrophy (LGMD) (Muscular Dystrophy Association)  
    Shoulder Injuries and Disorders/Related Issues ... Shoulder Injuries and Disorders ... Muscular Dystrophy/Specifics ... Muscular Dystrophy ... MDA is the #1 health nonprofit ...
  4. ... G, Hehr U, Winkler J, Topaloglu H. An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to ...
  5. ... both copies of the gene in each cell (autosomal recessive inheritance pattern).A small number of people with limb-girdle muscular dystrophy type 2F have developed a heart condition called ...
  6. Muscular Dystrophy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Muscular Dystrophy/Start Here ... Muscular Dystrophy ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Muscular dystrophy ( ...
  7. Limb-girdle muscular dystrophies are a large group of genetic ... types, only one parent needs to pass on the non-working gene ...
  8. What Are the Types and Symptoms of Muscular Dystrophy (MD)? From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Muscular Dystrophy/Specifics ... Muscular Dystrophy ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National Institutes ...
  9. ... The parents of an individual with an autosomal recessive condition each carry one copy of the altered gene, but they ... Muscular Dystrophy Genetic Testing Registry: Collagen 6-related myopathy ...
  10. ... ClinVar Allamand V, Guicheney P. Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 ...
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