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myotonic muscular dystrophy

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myotonic muscular dystrophy
[-ton′ik]
a severe form of muscular dystrophy marked by ptosis, facial weakness, and dysarthria. Weakness of the hands and feet precedes that in the shoulders and hips. Myotonia of the hands is usually present. Electromyography is helpful in establishing the diagnosis. Although there is no specific treatment, active and passive exercises are used to alleviate symptoms. Also called myotonia atrophica, Steinert's disease.


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0 million from the Muscular Dystrophy Association supporting the IPLEX(TM) Phase 2 Myotonic Muscular Dystrophy ("MMD") trial.
For years, neurologists have noticed a strange phenomenon: Patients afflicted by myotonic muscular dystrophy, a muscle-stiffening disorder, often have children with a more severe form of the disease.
Nasdaq:INSM), a biopharmaceutical company focused on the development and approval of drugs for the treatment of metabolic diseases with unmet medical needs, today announced the planned initiation of a 24-week, multi-center, randomized, double blind, placebo-controlled Phase II clinical trial with IPLEX[TM] in patients with Myotonic Muscular Dystrophy.
 
 
 
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