Johnston H A, Wilkinson J H, Withycombe W A, Raymond S
J Clin Pathol. 1966 May;19(3):250-6. doi: 10.1136/jcp.19.3.250.
In two families with severe sex-linked muscular dystrophy, high levels of alpha-hydroxybutyrate dehydrogenase (HBD), lactate dehydrogenase (LD), aspartate transaminase (AspT), aldolase, and creatine phosphokinase (CPK) were found in the sera of three young affected males. In both families the mother had a raised level of HBD activity. Four sisters of the three affected boys had raised serum enzyme levels, and they are regarded as presumptive carriers of the disease. Biopsy specimens of dystrophic muscle had LD and HBD contents which were significantly lower than those of control specimens, while the HBD/LD ratios were markedly greater. Muscle from two unaffected members of the same family also exhibited high ratios, indicating the presence of the electrophoretically fast LD isoenzymes, and this was confirmed by acrylamide-gel electrophoresis.
在两个患有严重性连锁肌营养不良症的家族中,在三名受影响的年轻男性血清中发现了高水平的α-羟丁酸脱氢酶(HBD)、乳酸脱氢酶(LD)、天冬氨酸转氨酶(AspT)、醛缩酶和肌酸磷酸激酶(CPK)。在两个家族中,母亲的HBD活性水平都有所升高。三名患病男孩的四个姐妹血清酶水平升高,她们被视为该疾病的推定携带者。营养不良肌肉的活检标本中LD和HBD含量明显低于对照标本,而HBD/LD比值明显更高。来自同一家族的两名未受影响成员的肌肉也表现出高比值,表明存在电泳快速LD同工酶,这通过丙烯酰胺凝胶电泳得到了证实。