Skibsted L, Westh H, Niebuhr E
Hum Genet. 1984;67(1):1-5. doi: 10.1007/BF00270550.
A woman with secondary amenorrhoea and an X long-arm deletion (pter----q21:) is described and compared with 30 adult non-mosaic, banded cases. Approximately 50% of the patients had gonadal dysgenesis associated with a higher frequency of short stature and "Turner stigmata" than in women with indication of ovarian activity. It is suggested that preservation of bands Xq26----28 may be decisive for normal ovarian function.
本文描述了一名患有继发性闭经且X染色体长臂缺失(pter----q21:)的女性,并将其与30例成年非嵌合、经染色体显带分析的病例进行了比较。约50%的患者存在性腺发育不全,与有卵巢活动迹象的女性相比,身材矮小和“特纳氏体征”的发生率更高。提示Xq26----28带的保留可能对正常卵巢功能起决定性作用。