德拉夏贝尔综合征:对临床和运动表现的影响

Sexes Pub Date : 2024-07-16 DOI:10.3390/sexes5030015
Paola Chiarello, Giuseppe Seminara, Sabrina Bossio, Luciana Sicilia, F. Greco, Paola Malatesta, Emanuela A Greco, Antonio Aversa
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引用次数: 0

摘要

青春期妇科炎症是一种良性疾病,大多会在发病后两年左右自然消失。如果伴有性腺功能减退,则可能提示性分化障碍。我们报告了一例伴有无精子症、小睾丸、高雌激素和高促性腺激素性性腺功能减退症的年轻男性(18 岁)妇科乳腺增生症。他的核型为 46,XX,通过荧光原位杂交(FISH)检测 SRY(性别决定区 Y),发现该基因位于短臂的末端区域,断裂点可能在 Xp22.3 和 Yp11.3。本文讨论了睾酮替代疗法对性别分化障碍和体能表现的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
De La Chapelle Syndrome: Clinical and Physical Performance Implications
Gynecomastia in adolescence is a benign condition that mostly disappears spontaneously within approximately two years from onset. When it is associated with hypogonadism, it may suggest a disorder of sexual differentiation. We report the case of a young man (18 years old) with gynecomastia associated with azoospermia, small testes, hyperestrogenism and hypergonadotropic hypogonadism. A karyotype 46,XX was found, and searching for SRY (sex-determining region Y) by fluorescence in situ hybridization (FISH) highlighted the presence of the gene on the terminal region of the short arm, with breakpoints likely in Xp22.3 and Yp11.3. Implications of testosterone replacement therapy with respect to sex differentiation disorder and to physical performance are discussed.
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