家族性横紋筋融解症
WordNet
- relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
- occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible
PrepTutorEJDIC
- 家族の,家族特有の / 違伝的な,血統にあらわれる
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English Journal
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- Familial paroxysmal rhabdomyolysis with myoglobinuria is a rare and life-threatening disease of young children, of unknown aetiology. Attacks bear no relation to exercise, are usually triggered by intercurrent infections and are often severe. The authors describe two cases and suggest plans for the prevention and management of attacks.
- Familial dysautonomia (FD, OMIM# 223900) is an autosomal recessive disease featured by impaired pain and temperature perception and lack of functional muscle spindles. After 3 FD patients presented with rhabdomyolysis in a short time span, we aimed to ...
- Rhabdomyolysis, which literally means striated muscle dissolution or disintegration,1 is a potentially lethal clinical and biochemical syndrome.2 Approximately 26,000 cases of rhabdomyolysis are ...
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- 英
- familial myoglobinuria
- 同
- 家族性横紋筋融解症 familial rhabdomyolysis
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- 関
- family、family member、household、kindred