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甘油激酶缺芝(GKD)是一种 X 连锁隐性遗传性状,其发生与先天性肾上腺发育不全(AH)以及伴有或不伴有先天性肌营养肌病的发育延缓有关。已报道过几个病人,发现他们在染色体区域Xp_(21)有细胞学缺乏和/或 DNA 标记缺失,此 DNA标记是处在 XP_(21)带上的 Duchenne 肌营养不良(D-
GKD is an X-linked recessive inherited trait associated with congenital adrenal hypoplasia (AH) and developmental delay associated with or without congenital muscular myopathy. Several patients have been reported and found to be cytologically deficient and / or lacking a DNA marker at the chromosomal region Xp_ (21). The DNA marker is Duchenne’s muscular dystrophy (D-