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性发育障碍:分类、综述及对生育能力的影响

Disorders of Sex Development: Classification, Review, and Impact on Fertility.

作者信息

Acién Pedro, Acién Maribel

机构信息

Departmentof Gynecology, Miguel Hernández University, San Juan Campus, 03550 San Juan, Alicante, Spain.

Obstetrics and Gynecology. San Juan University Hospital. San Juan Campus, 03550 San Juan, Alicante, Spain.

出版信息

J Clin Med. 2020 Nov 4;9(11):3555. doi: 10.3390/jcm9113555.

Abstract

In this review, the elements included in both sex determination and sex differentiation are briefly analyzed, exposing the pathophysiological and clinical classification of disorders or anomalies of sex development. Anomalies in sex determination without sex ambiguity include gonadal dysgenesis, polysomies, male XX, and Klinefelter syndrome (dysgenesis and polysomies with a female phenotype; and sex reversal and Klinefelter with a male phenotype). Other infertility situations could also be included here as minor degrees of dysgenesis. Anomalies in sex determination with sex ambiguity should (usually) include testicular dysgenesis and ovotesticular disorders. Among the anomalies in sex differentiation, we include: (1) males with androgen deficiency (MAD) that correspond to those individuals whose karyotype and gonads are male (XY and testes), but the phenotype can be female due to different hormonal abnormalities. (2) females with androgen excess (FAE); these patients have ovaries and a 46,XX karyotype, but present varying degrees of external genital virilization as a result of an enzyme abnormality that affects adrenal steroid biosynthesis and leads to congenital adrenal hyperplasia; less frequently, this can be caused by iatrogenia or tumors. (3) Kallman syndrome. All of these anomalies are reviewed and analyzed herein, as well as related fertility problems.

摘要

在本综述中,我们简要分析了性别决定和性别分化所包含的要素,揭示了性发育障碍或异常的病理生理和临床分类。无性别模糊的性别决定异常包括性腺发育不全、多体性、男性XX以及克兰费尔特综合征(具有女性表型的发育不全和多体性;以及具有男性表型的性反转和克兰费尔特综合征)。其他不育情况也可作为轻度发育不全包含在此处。伴有性别模糊的性别决定异常通常应包括睾丸发育不全和卵睾症。在性别分化异常中,我们包括:(1)雄激素缺乏的男性(MAD),对应于那些核型和性腺为男性(XY和睾丸),但由于不同的激素异常,表型可为女性的个体。(2)雄激素过多的女性(FAE);这些患者有卵巢且核型为46,XX,但由于影响肾上腺类固醇生物合成并导致先天性肾上腺皮质增生的酶异常,出现不同程度的外生殖器男性化;较少见的情况是,这可能由医源性因素或肿瘤引起。(3)卡尔曼综合征。本文对所有这些异常情况以及相关的生育问题进行了综述和分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9100/7694247/94efc9bcbf6d/jcm-09-03555-g001.jpg

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