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The Phenotype of Limb-Girdle Muscular Dystrophy Type 21
Neurol 60:1246-1251,1230, Poppe,M.,et al, 2003
See this aricle in Pubmed

Article Abstract
Mutations in the fukutin-related protein gene FKRP cause limb-girdle muscular dystrophy (LGMD21) as well as a form of congenital muscular dystrophy (MDC1C). LGMD21 due to FKRP mutations appears to be a relatively common cause of LGMD, with respiratory and cardiac failure as prominent complications.
 
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calf hypertrophy
cardiomyopathy
creatine phosphokinase(CPK)elevated
muscle hypertrophy
muscular dystrophy
muscular dystrophy,cardiovascular changes with
muscular dystrophy,limb-girdle
neurologic disease,diagnoses of
pseudohypertrophy
respiratory failure
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