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Adornato等发现18例进行性肌营养不良病(DMD)中有14例患肌红蛋白贫血,16例中有10例是携带者.Norregaard Hansen等用放射免疫法对肌红蛋白5μg/l作为一个敏感度.他们发现在8个患儿中有7例血清肌红蛋白水平增加,并有两例是肯定的携带者.在肌红蛋白与肌酐磷酸激酶(CPK)活性之间无矛盾.建议测定胎血或羊水中的肌红蛋白,可以产前诊断DMD.T?r?k等报告羊水中肌红蛋白增高的1例.此胎儿生后显示DMD特征,其母22岁初孕,于孕16周行羊水穿刺,血清CPK水平高,被注意到是一个
Adornato et al found that 14 of 18 patients with progressive muscular dystrophy (DMD) had myoglobin anemia and 10 of 16 patients were carriers.Norregaard Hansen et al. Used radioimmunoassay for myoglobin 5 μg / l as one Sensitivity, they found that 7 of 8 children had increased levels of serum myoglobin and two were positive carriers, and there was no contradiction between myoglobin and creatinine phosphokinase (CPK) activity. Fetal blood or amniotic fluid in amniotic protein, prenatal diagnosis of DMD.T? R? K and other reports of amniotic fluid amniotic increased in 1 case of this fetus after birth showed the characteristics of DMD, the mother of the first 22-year-old pregnant in pregnancy 16 Week amniocentesis, high level of serum CPK, was noticed is one