[Lowe's syndrome (author's transl)].

Archives d'ophtalmologie Pub Date : 1977-01-01
C Jezegabel, G Duprey, E Zafimehy
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Abstract

Concerning the clinical study, the oculo-cerebro-renal syndroms are well drawn and we nearly could say there is no syndrome of Lowe without a cataract. This conviction puts aside some oculo-cerebro-renal syndroms occured to female and easily called "Lowe's Syndrom". The glaucoma which exists in half of the cases, is scarcely a mechanical type, sometimes it is an usual congenital type with membrane of Barkan, but the more frequently, it is secondary to an alteration of all constitutive elements of the anterior uvea and of the camerular angle. Concerning inheritance, the absence of female cases among the PF observations confirm the recessive transmission attached to the sex, which is, in fact, definively established. Though the search of hererozygote females after an ophtalmological or biochimical observation has no absolute value, it anyway adds some very precious genetic requirements. Concerning the etio-pathogenic study, as we tried to show, the authors agree in simultaneous and contemporary appearance, between the 4th and the 6th month of the intra-uterine life of oculo-cerebro-renal troubles of Lowe's Syndrom and in the existence of a common factor, probably a genetic one. Anyway, we still have to precise the nature of the gene and the inter relations existing between the three injures.

[劳氏综合症(作者译)]。
在临床研究方面,眼-脑-肾综合征已被很好地描绘出来,我们几乎可以说没有无白内障的Lowe综合征。这一信念排除了发生在女性身上的一些容易被称为“罗氏综合症”的眼-脑-肾综合征。半数病例的青光眼几乎不是机械性青光眼,有时是常见的先天性巴坎膜青光眼,但更常见的是,青光眼继发于葡萄膜前和照相机角的所有组成部分的改变。关于遗传,在PF观察中没有女性病例证实了与性别相关的隐性传播,这实际上是明确成立的。虽然在眼科或生化观察后寻找雌性杂合子没有绝对价值,但它无论如何增加了一些非常宝贵的遗传要求。关于病因研究,正如我们试图表明的那样,作者同意在同时和当代的出现,在劳氏综合征的眼-脑-肾疾病的子宫内生活的第4和第6个月之间,存在一个共同的因素,可能是遗传因素。不管怎样,我们还得弄清楚基因的性质以及这三处伤之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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