重型β-地中海贫血的青春期女性患者下丘脑-垂体-性腺轴的功能

来源 :世界核心医学期刊文摘(妇产科学分册) | 被引量 : 0次 | 上传用户:adfda
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Objective: To evaluate the function of the hypothalamic-pituitary-gonadal axis in adolescent female patients with beta-thalassemia major. Materials and methods: A prospective study of the function of the hypothalamic-pituitary-gonadal axis function of 31 beta-thalassemia major females aged between 13 and 22 years and in 12 control females aged between 12 and 22 years. All were treated at Princess Rahma Teaching Hospital, Irbid, Northern Jordan between April 2001 and April 2003. Results: Of the 31 beta-thalassemia major females, 13 (41.9% ) had delayed puberty. Hypothalamic- pituitary-ovarian axis dysfunction was found in 15 patients (48.4% ). Twelve patients (38.7% ) had hypogonadotropic hypogonadism and 5 (16.1% ) had ovarian failure. High levels of serum ferritin were significantly higher in patients with delayed puberty. Conclusion: Pituitary and ovarian dysfunction are common problems in beta- thalassemia major patients. The main possible cause is iron overload. This stresses the need for intensive and regular use of chelation therapy to prevent damage to the hypothalamic-pituitary- ovarian axis. Objective: To evaluate the function of the hypothalami-pituitary-gonadal axis in adolescent female patients with beta-thalassemia major. Materials and methods: A prospective study of the function of the hypothalami-pituitary-gonadal axis function of 31 beta-thalassemia major females aged between 13 and 22 years and in 12 control females aged between 12 and 22 years. All were treated at Princess Rahma Teaching Hospital, Irbid, Northern Jordan between April 2001 and April 2003. Results: Of the 31 beta-thalassemia major females, 13 (41.9%) had delayed puberty. Hypothalamic-pituitary-ovarian axis dysfunction was found in 15 patients (48.4%). Twelve patients (38.7%) had hypogonadotropic hypogonadism and 5 (16.1%) had ovarian failure. High levels of serum ferritin were significantly higher in patients with delayed puberty. Conclusion: Pituitary and ovarian dysfunction are common problems in beta- thalassemia major patients. The main possible cause is iron overload. This stresses the n eed for intensive and regular use of chelation therapy to prevent damage to the hypothalamic-pituitary-ovarian axis.
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