Genetic Myopathies (eg, Muscular Dystrophies)
Clinical Pathology
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Musculoskeletal & Dermatologic Pathologies
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Developmental Disorders
Q. Which of the following manifests with myotonia from a CLCN1 gene mutation?
a
Myotonia Congenita
b
McArdle Disease (Glycogen Storage Disease Type V)
c
Myotonic Dystrophy, Type 1
d
Myotonic Dystrophy, Type 2
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