1例报告:女性重度β -地中海贫血不孕症的治疗

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引用次数: 1

摘要

β-地中海贫血是由遗传介导的血红蛋白β-珠蛋白链缺失引起的。它是一种常染色体隐性遗传疾病,会导致需要长期输血的严重疾病。下丘脑-垂体-卵巢轴受损主要导致此类患者不孕。这篇病例报告介绍了一名26岁的女性,一名已知的严重β地中海贫血病例,在怀孕前每月接受输血。患者在巴林国防军皇家医疗服务医院寻求原发性不孕治疗咨询。患者接受了两次宫内受精(IUI)试验。目的是通过给胚胎植入使用促性腺激素来增加子宫内膜厚度。总之,宫内节育器联合促性腺激素用于卵巢刺激已显示出成功。关键词:人工授精,β地中海贫血,性腺功能低下,不孕,妊娠
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case Report: Infertility Treatment of a Female with Beta-thalassemia Major
Beta-thalassemia is caused by a genetically mediated deletion of beta-globin chain of hemoglobin. It is an autosomal recessive disease, which causes a severe medical condition that requires longterm blood transfusions. An impaired hypothalamic-pituitary-ovarian axis mainly causes infertility in such patients. This case report presents a 26-year-old female, a known case of beta-thalassemia major, that received monthly blood transfusions before conceiving. The patient sought consultation for the treatment of primary infertility at Bahrain Defence Force Royal Medical Services (BDF-RMS) Hospital. The patient underwent two trials of intrauterine insemination (IUI). The goal was to build up endometrial thickness by gonadotrophins administration for embryo implantation. To conclude, IUI combined with gonadotrophins for ovarian stimulation has shown success. Keywords: Artificial Insemination, Beta-Thalassemia, Hypogonadism, Infertility, Pregnancy
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