Enzymatic Activity in Serum Obtained from Muscular Dystrophic Patient's Family
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One hundred sixty three cases, (mother, 83; father, 65; sister, 6; brother, 9;) who have one or more Duchenne type muscular dystrophy patient in their family and no clinical finding of myopathy at the time of examination, were studied.The following enzymatic activity of serum obtained from these people were measured.Aldolase (ALD), Glutamic oxaloacetic transaminase (GOT), Glutamic pyruvic transaminase (GPT), Lactic dehydrogenase (LDH), Creatine phosphokinase (CPK), (1) The enzymatic activity in serum obtained from patient's mothers showed almost normal value on ALD, LDH and GPT, but 30.6 percent of mothers on GOT and 37.3 percent on CPK showed abnormal value. These mother were divided into three groups by a type of inheretance; possible carrier type, probable carrier type, definite carrier type. Enzymatic activity of CPK, at each group, showed abnormal value; 31.6 percent at possible carrier, 46.6 percent at probable carrier, 54.5 percent at definite carrier.(2) The enzymaic activity in serum obtained from patient's fathers showed normal value on ALD, and LDH, but 24.2 percent of fathers on GOT, 13.9 percent on GPT, 13.7 percent on CPK showed abnormal value.(3) The enzymatic activity in serum obtained from patient's sister showed abnormal value at 33.3 percent on GOT, 50.0 percent on CPK, but another enzymatic activity were normal.(4) The enzymatic activity in serum obtained from patient's brothers showed abnormal value at 11.1 percent on CPK, but anothers were normal.
- 一般社団法人 国立医療学会の論文
一般社団法人 国立医療学会 | 論文
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