Which clinical history findings are characteristic of autosomal-recessive limb-girdle muscular dystrophy 2O (LGMD2O)?

Updated: Aug 15, 2019
  • Author: Monica Saini, MD, MBBS, MRCP(UK); Chief Editor: Nicholas Lorenzo, MD, MHA, CPE  more...
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Answer

LGMD2O (LGMDR15  POMGnT1; 1p32)

This disease is allelic with muscle-eye-brain disease (see Congenital Muscular Dystrophy).

Rare cases are described with a LGMD phenotype. Calf hypertrophy has been noted


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