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Results 1 - 10 of 16 for "Limb-girdle" muscular "dystrophy," recessive
  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. ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 7; LGMDR7 MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE ...
  3. ... Hehr U, Winkler J, Topaloglu H. An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to ...
  4. ... 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 ...
  5. Limb-girdle muscular dystrophies are a large group of genetic ... types, only one parent needs to pass on the non-working gene ...
  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. 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 ...
  8. 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 ...
  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. ... ANO5 gene have been identified in people with limb-girdle muscular dystrophy type 2L. Limb-girdle muscular dystrophy is a group of related disorders characterized by ...
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