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闭经患者细胞遗传学检查的临床意义
引用本文:杨瑞芳,王明毅,王济周. 闭经患者细胞遗传学检查的临床意义[J]. 现代妇产科进展, 2001, 10(2): 114-116
作者姓名:杨瑞芳  王明毅  王济周
作者单位:山东大学齐鲁医院围产医学中心
摘    要:目的 :分析闭经患者细胞遗传学的检查结果及其临床意义。方法 :对每例闭经患者进行常规妇科检查及细胞遗传学检查 ,包括外周血淋巴细胞培养制备染色体 ,G显带与C显带 ,必要时进行高分辨显带或银染处理 ,或同时用内分泌及超声检查。结果 :2 33例闭经患者中 ,88例染色体异常 ,占 37 78% ,包括染色体数异常、缺失、倒位及嵌合。结论 :染色体异常是闭经的主要原因之一 ,染色体核型分析对确诊闭经的病因、治疗及确定预后必不可少

关 键 词:闭经  细胞遗传学  染色体分析
文章编号:1004-7379(2001)02-0114-03
修稿时间:2000-10-12

The analysis of cytogenetic abnormalities for patients with amenorrhea
YANG Ruifang,Wang Mingyi,Wang Jizhou. The analysis of cytogenetic abnormalities for patients with amenorrhea[J]. Current Advances In Obstetrics and Gynecology, 2001, 10(2): 114-116
Authors:YANG Ruifang  Wang Mingyi  Wang Jizhou
Affiliation:Yang Ruifang,Wang Mingyi,Wang Jizhou. Genetic Lab.of Perinatalologic Centre of QiLu Hospital of Shandong University,Jinan,250012
Abstract:Objective: To analyse the cytogenetic examinations and their clinical significance for patients with amenorrhea. Methods: The routing gynecologic examination and cytogenetics were performed including pheripheral blood lymphocytes culture for chromosome, and G-banding, C-banding, or if necessary, high resolution banding and silver-staining were treated. In sometimes, endocrine and ultrasound examination were performed simultaneously. Results: There were 88 cases with chromosome abnormally in 233 cases of amenorrhea,account for 37.78%, including number abnormality, deletion, inversion and mosaic type. Conclusions: Chromosome abnormality is one of the main causes of amenorrhea. Karyotype analysis of chromosome are absolutely necessary methods for seeking the cause, therapy and prognosis of patients with amenorrhea.
Keywords:Amenorrhea   Cytogenetics   Chromosomal analysis
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