| myotonic dystrophy |
an inherited (autosomal dominant) neuromuscular disorder that occurs in adults, characterized by progressive muscle weakness and wasting and myotonia; onset is usually in the third decade
출처: depts.washington.edu/pwdlearn/web/glossary/glossar...
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| myotonic dystrophy |
an inherited autosomal dominant disorder that causes muscle weakness and myotonia (inability of muscles to relax after use), which becomes more severe over time.
출처: www.uchicagokidshospital.org/online-library/conten...
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| myotonic dystrophy |
a progressive disorder characterized by by generalized weakness, the inability of the muscles to relax after contracting, and wasting of the muscles in the hands, face, feet and neck initially. Also known as Steinert's disease or Dystrophia Myotonica. For more information see International Myotonic Dystrophy Organization
출처: kid-power.org/definitions.html
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| myotonic atrophy |
Myotonia congenita.
출처:
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| myotonic d. |
high frequency repetitive discharges seen in myotonia and evoked by insertion of a needle electrode, percussion of a muscle, or stimulation of a muscle or its motor nerve; characterized by waxing and waning of frequency and amplitude. There are two types: one with biphasic spike potentials resembling fibrillation potentials and one with waves resembling positive sharp waves.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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