Suppr超能文献

类固醇硫酸酯酶缺乏症的临床谱:X连锁隐性鱼鳞病、出生并发症和隐睾症。

Clinical spectrum of steroid sulfatase deficiency: X-linked recessive ichthyosis, birth complications and cryptorchidism.

作者信息

Traupe H, Happle R

出版信息

Eur J Pediatr. 1983 Mar;140(1):19-21. doi: 10.1007/BF00661898.

Abstract

When boys affected with steroid sulfatase deficiency are delivered, the lack of the enzyme in the placenta may cause birth complications. In postnatal life this gene defect gives rise to X-linked recessive ichthyosis. In a series of 25 patients birth complications were reported in 9 cases. Of these boys, 4 displayed bilateral inguinal cryptorchidism and one was affected unilaterally. In a further boy we observed unilateral inguinal cryptorchidism without a history of birth complications. In one patient who had been delivered by forceps, abdominal bilateral cryptorchidism resulted in severe hypogenitalism. A review of the literature revealed 30 cases with X-linked recessive ichthyosis displaying hypogenitalism or cryptorchidism or both. In conclusion, cryptorchidism should be considered as a further clinical manifestation of steroid sulfatase deficiency.

摘要

患有类固醇硫酸酯酶缺乏症的男婴出生时,胎盘中缺乏该酶可能会导致出生并发症。在出生后的生活中,这种基因缺陷会引发X连锁隐性鱼鳞病。在一组25例患者中,有9例报告了出生并发症。在这些男孩中,4例表现为双侧腹股沟隐睾,1例为单侧隐睾。在另一名男孩中,我们观察到单侧腹股沟隐睾,且无出生并发症史。在一名使用产钳分娩的患者中,双侧腹部隐睾导致严重生殖器发育不全。文献回顾显示,30例X连锁隐性鱼鳞病患者表现出生殖器发育不全或隐睾或两者皆有。总之,隐睾应被视为类固醇硫酸酯酶缺乏症的另一种临床表现。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验