（一）肌营养不良假肥大型（pseudohy pertrophic muscular dystrophy） 属X陆续锁隐性遗传，按照发病年数和病情成长纪律可分为下列两型：
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目的探讨同患假肥大型肌营养不良症(DMD)兄妹的临床以及实验室检查特点。
Objective To investigate the clinical and lab features of sibling brother and sister both with Duchenne muscular dystrophy (DMD).
目的为探讨假肥大型肌营养不良症（DMD）基因内含子的核苷酸序列特点与存在于内含子中的多个断裂点的关系。
Objective The purpose of the study was to investigate the relationship between the character of nucleic acids and the multiple breakpoints in the introns of DMD gene.
研究假肥大型肌营养不良(DMD)病人肌酸激酶同工酶(CK - MB)及其亚型的变化，为早期诊断和判定病情提供依据。
To study the changes of creatine kinase isoenzyme (CK-MB) and its isoforms in patient with DMD for the purpose of early diagnosis and evaluation, a discontinuous buffer system was used.
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