bn:00056630n
Noun Concept
Categories: Muscular dystrophy, Trinucleotide repeat disorders, Myoneural junction and neuromuscular diseases, Autosomal dominant disorders, All articles needing additional references
EN
myotonic muscular dystrophy  myotonic dystrophy  myotonia atrophica  Steinert's disease  CMyD
EN
A severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant WordNet 3.0
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EN
A severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant WordNet 3.0 & Open English WordNet
Myotonic dystrophy is a type of muscular dystrophy, a group of genetic disorders that cause progressive muscle loss and weakness. Wikipedia
A chronic muscle-wasting disease Wikipedia Disambiguation
Long term genetic disorder that affects muscle function Wikidata
Myotonic dystrophy. Wiktionary
A chronic, slowly progressing, inherited multisystemic disease, characterized by muscular dystrophy, cataracts, heart conduction defects, endocrine changes, and myotonia. Wiktionary