Results 1 - 5 of 5 for "Limb-girdle" muscular "dystrophy," type 1A
  1. Rare Diseases and Related Terms From the National Institutes of Health (Office of Rare Diseases)  
    ... See Hereditary diffuse leukoencephalopathy with spheroids * Autosomal dominant limb-girdle muscular dystrophy type 1A - See Limb-girdle muscular dystrophy type 1A * Autosomal ...
  2. ... Registry: Limb-girdle muscular dystrophy Genetic Testing Registry: Limb-girdle muscular dystrophy, type 1A Genetic Testing Registry: Limb-girdle muscular dystrophy, type ...
  3. ... same region as the gene that’s defective in limb-girdle MD type 1A. Symptoms first appear between about 35 and 60 years of age and include weakness of the hands, legs or voice. Difficulty in swallowing may be a feature. Distal muscular dystrophy refers to a group of disorders that primarily ...
  4. ... congenital muscular dystrophies and is sometimes called congenital muscular dystrophy type 1A. Affected infants have severe muscle weakness, lack of ... disorder are milder than in the early-onset type and are similar to those of a ... dystrophies. In late-onset LAMA2 -related muscular dystrophy, the ...
  5. Charcot-Marie-Tooth and Related Diseases (Muscular Dystrophy Association) - PDF  
    ... Steinert disease) Duchenne muscular dystrophy Becker muscular dystrophy Limb-girdle muscular ... disease) Intermediate spinal muscular atrophy ( ...
Refine by Type
  • All Results (5)
  • Health Topics
  •  External Health Links (5)
  • Drugs and Supplements
  • Medical Encyclopedia
  • Videos and Tutorials
  • News
  • MedlinePlus Magazine
  • Other Resources
  • Multiple Languages