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首页> 外文期刊>Case Reports in Obstetrics and Gynecology >Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review
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Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review

机译:Malouf综合征伴促性腺激素性性腺功能减退症和心肌病:两例报道并文献复习

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摘要

Malouf syndrome is a very rarely encountered syndrome which was first diagnosed in 1985 upon the examination of two sisters, with findings of hypergonadotropic hypogonadism, dilated cardiomyopathy, blepharoptosis, and broad nasal base. Later on, Narahara diagnosed another sporadic case with the same findings. A survey of relevant literature leads us to three women cases in total. Here we present two cases of Malouf syndrome and literature review.
机译:Malouf综合征是一种很少见的综合征,于1985年在对两个姐妹进行检查后首次被诊断出,发现有促性腺功能低下性腺功能减退症,扩张型心肌病,睑缘炎和鼻基宽。后来,奈良原(Narahara)诊断了另一例具有相同发现的零星病例。通过对相关文献的调查,我们总共发现了三个女性案例。在这里,我们介绍两例马洛夫综合征和文献复习。

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