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作 者:刘德云[1] 杨俐琦[1] 蒋惠珍[1] 张志红[1] 周美玲[1] 李桢[1]
出 处:《中国妇幼保健》2009年第21期2969-2970,共2页Maternal and Child Health Care of China
摘 要:目的:提高临床医生对Turner综合征的认识。方法:分析Turner综合征临床和辅助检查特点。结果:所有患者都有矮小,乳房发育不良或不发育,同时伴有黑痣增多5例,发际低5例,眼裂不等大1例,眼睑下垂4例,鼻梁低平2例,颈蹼4例,乳头间距明显增宽5例,明显肘外翻4例。性腺BUS:2例子宫、卵巢发育不良,3例子宫卵巢显示不清,3例子宫、卵巢未显示。染色体核型分析:45,XO4例;45XO/46XX2例;46,X,i(Xq)1例;46,X,del(Xq)1例。骨龄:8例均提示骨龄落后,平均1~3年。其中2例有第4掌骨短小。生长激素激发试验:1例激发试验生长激素水平正常,5例生长激素部分缺乏,2例生长激素完全缺乏。结论:Turner综合征具有典型的临床特点,临床发病率高,提高对本病认识,及时进行染色体核型分析可以确诊。早期诊断、及时治疗对增加患者终身高,提高Turner综合征患者的生活质量有重要意义。Objective: To improve the cognition of clinical doctors to Turner syndrome. Methods: The clinical and examination characteristics of Turner syndrome were analysed. Results: All the cases were short, mammary dysplasia or agenesis, and 5 cases of more moles, 5 cases of low hairline, 1 case of different ocali rimae, 4 cases of blepharoptosis, 2 cases of low and flat bridge of the nose, 4 ca- ses of webbed neck, 5 eases of wide distance of two nipples, 4 cases of valgus eubitus were found. Sex glands BUS found 2 cases of hypogenesis of uterus and ovary, 3 cases of indiscernible uterus and ovary, 3 cases of invisible uterus and ovary. Karyotype analysis found 4 ca- ses of 45, XO; 2 cases of45XO/46 XX; 1 case of 46, X, i (Xq) and 1 case of 46, X, del (Xq). Skeletal age detection indicated that all the 8 cases had laggard skeletal age, the mean time was 1 - 3 years, and 2 cases were found with a shorter fourth metacarpal. Growth hormone provocative test showed that 1 case was nrmal, 5 cases were deficiency partially, 2 cases were deficiency absolutely. Con- clusion : The clinical characteristics of Turner syndrome are typical and its incidence is high, timely karyotype analysis is a method of accurate diagnosis. Early diagnosis and early therapy are important for improving the life quality of the patients.
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