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首页> 外文期刊>Indian Journal of Human Genetics >Chromosomal abnormalities and hormonal disorders of primary amenorrhea patients in Egypt
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Chromosomal abnormalities and hormonal disorders of primary amenorrhea patients in Egypt

机译:埃及原发性闭经患者的染色体异常和激素紊乱

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摘要

BACKGROUND: Primary amenorrhea is defined as the absence of menstruation and secondary sexual characteristics in phenotypic women aged 14 years or older. Hormonal disorders are main causes of primary amenorrhea. Common hormonal cause of primary amenorrhea includes pituitary dysfunction and absent ovarian function. The aim of this study was to estimate the incidence and types of chromosomal abnormalities in patients with primary amenorrhea in Egypt. MATERIALS AND METHODS: Chromosomal analysis and hormonal assay were carried out on 223 patients with primary amenorrhea that were referred from different parts of Egypt to Cytogenetic laboratory of Genetic Unit, Children Hospital Mansoura University, from July 2008 to December 2010. FISH technique was carried out in some of cases to more evaluation. RESULTS: The frequency of chromosomal abnormalities was 46 (20.63%) in primary amenorrhea patients. The chromosomal abnormalities can be classified into four main types. (1) The numerical abnormalities of the X?chromosome were detected in 23 (50 %). (2) Structural abnormalities of the X chromosome were detected in 11 (23.91%). (3) Mosaicism of X chromosome was found in 10 (21.74%). (4) Male karyotype 46, XY was presented in 2 (4.35%). CONCLUSION: The present study showed that karyotype and FISH are necessary to detect the causes of primary amenorrhea. This study also revealed the incidence of chromosomal abnormalities in women with primary amenorrhea in Egypt is similar to that reported in previous literatures.
机译:背景:原发性闭经的定义是:年龄在14岁或以上的表型女性没有月经和继发性征。激素障碍是原发性闭经的主要原因。激素引起原发性闭经的常见原因包括垂体功能障碍和卵巢功能缺失。这项研究的目的是评估埃及原发性闭经患者的染色体异常发生率和类型。材料与方法:于2008年7月至2010年12月在埃及不同地区转诊至曼索拉大学儿童医院遗传科细胞遗传学实验室的223例原发性闭经患者进行了染色体分析和激素测定。在某些情况下需要更多评估。结果:原发性闭经患者的染色体异常发生频率为46(20.63%)。染色体异常可分为四种主要类型。 (1)在23(50%)中检测到X染色体的数值异常。 (2)检测到X染色体的结构异常的11例(23.91%)。 (3)X染色体的镶嵌率为10(21.74%)。 (4)男性2型(4.35%)的染色体核型为46,XY。结论:本研究表明核型和FISH对于检测原发性闭经的原因是必要的。这项研究还揭示了埃及原发性闭经妇女的染色体异常发生率与先前文献报道的相似。

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