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[Pseudo-exfoliative fibrillopathy in eastern Algeria. Epidemiologic and statistical study]. 阿尔及利亚东部假性剥脱性纤维病。流行病学和统计研究]。
O S Boukoffa, J Flament, D Hartani

The systematic examination of 1440 patients of more than 40 years old divided into two groups of 607 hospitalised patients and 833 consultants has revealed the exceptionally high frequency of the pseudo-exfoliative disease in the East of Algeria. In fact this syndrome is find in 25% of the cases. The analysis relates the different epidemiology criteria: age, topography, geographic factors and biomicroscopic characters. The association to the glaucoma of this syndrome forms the subjects of a study which details particularly its frequency, its different clinical forms, the factors of the intraocular pressure and the evolution under treatment. The authors have compared this study to those wHich have been described in literature.

对1440名40岁以上的患者进行系统检查,分为两组(607名住院患者和833名顾问),发现阿尔及利亚东部假性剥脱性疾病的发病率异常高。事实上,25%的病例都有这种症状。分析了不同的流行病学标准:年龄、地形、地理因素和生物显微镜特征。该综合征与青光眼的关系形成了一项研究的主题,该研究特别详细说明了其频率,其不同的临床形式,眼压因素和治疗过程中的演变。作者将这项研究与文献中描述的研究进行了比较。
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引用次数: 0
[The progeny of the two protan and deutan families described by Franceschetti and Klein (1949, 1956), one generation later. Genealogy, color vision and genomic DNA]. [Franceschetti和Klein(1949, 1956)描述的两个protan和deutan家族的后代,一代之后。]族谱,色觉和基因组DNA]。
A Roth, D Klein, F Paccolat, D Hermès, M Pelizzone, J L Mandel, R Feil

The progeny of the couple of which the husband was protanope and the wife deuteranope (Franceschetti, 1949) has been examined (3 generations) in 1986 and 1987. This couple had 4 children, of which 3 sons are deutan and 1 daughter, a double carrier, is phenotypically normal. This girl, in her turn and in exemplary fashion, has 3 children: 1 daughter, being simple carrier, is phenotypically normal, 1 son is protan and 1 son deutan. The study of the genomic DNA of 3 normal subjects reveals the presence of two genes responsible for green and one gene responsible for red; the genomic DNA of a protanomalous subject shows a modification of the gene for red, while that of two deuteranopes shows absence of genes responsible for green. The descent of the second couple in which the husband was deuteranope and the wife protanope (Franceschetti and Klein, 1956) is exclusively of female sex. Therefore it comprises only phenotypically normal persons.

1986年和1987年对丈夫为protanope,妻子为deuteranope (Franceschetti, 1949)夫妇的后代(3代)进行了检查。这对夫妇有4个孩子,其中3个儿子是德国人,1个女儿是双携带者,表型正常。这个女孩,反过来,以典型的方式,有三个孩子:一个女儿,是简单的携带者,是典型的正常,一个儿子是蛋白质和一个儿子是多变性。对3名正常人的基因组DNA的研究发现,存在两个负责绿色的基因和一个负责红色的基因;一名原异形动物的基因组DNA显示出红色基因的修饰,而两名后蜥蜴的基因组DNA显示出绿色基因的缺失。第二对夫妇的后裔,丈夫是deuteranope,妻子是protanope (Franceschetti and Klein, 1956),完全是女性。因此,它只包括表型正常的人。
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引用次数: 0
[Electroretinographic problems in the diagnosis of diseases of the cones and macula]. 视网膜电图在锥、黄斑病变诊断中的问题
J C Hache, S Defoort, B Puech, F Bale, E Mancel

From series of clinical cases, the authors expose how ERG is an essential element for the diagnosis of cone dysfunction with or without macular involvement. They show that to obtain an accurate diagnosis, precise proceedings must be chosen, using stimulation technics correctly selected. They study the advantage of focal or wide stimulations, of the level of the intensity of the stimulation and of the different colored filters. They propose a proceeding for adults examination. For young children, they discuss the advantages and limits of a particular proceeding.

从一系列的临床病例中,作者揭示了ERG是诊断有或没有黄斑受累的视锥细胞功能障碍的基本要素。他们表明,要获得准确的诊断,必须选择精确的程序,使用正确选择的刺激技术。他们研究了焦点刺激或广泛刺激的优势,刺激强度的水平和不同颜色的过滤器。他们提出了成人考试的程序。对于年幼的孩子,他们讨论特定程序的优点和局限性。
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引用次数: 0
[Current treatment of simple retinal detachment. Advantages and inconveniences of permanent and temporary scleral buckling compared with gas expansion of the retina]. 单纯性视网膜脱离的治疗现状。永久性和暂时性巩膜屈曲与视网膜充气扩张的优缺点比较[j]。
A Urrets-Zavalia

Limited cryopexy followed by attachment to the sclera of a small, cylindrical silicone sponge at the site of the tear leads in most cases to a prompt reduction of any non-complicated rhegmatogenous detachment. As a rule, no drainage of the subretinal fluid is necessary. If an inflatable silicone balloon is used in lieu of a permanent tampon, the short-term result may be the same; renewed tension of the vitreous bands which caused the tear may lead, however, to a redetachment in the long term. Intravitreal injection of an insoluble gas (mostly perfluoro-propane or hexafluorure ) may also be used to close up the tear, while cryopexy or photocoagulation are to be applied to seal its borders. After resorption of the gas the vitreous bands will again be under tension, and the risk of a recurrence appear. The fact that the vitreous chamber must be entered entails, on the other hand, some risks of its own.

在大多数情况下,在巩膜撕裂处附着一个小的圆柱形硅胶海绵,然后进行有限的冷冻固定,可以迅速减少任何非复杂的孔源性脱离。通常,不需要引流视网膜下液。如果使用可充气的硅胶球代替永久性卫生棉条,短期效果可能是一样的;然而,造成撕裂的玻璃体带再次紧张可能导致长期的再脱离。玻璃体内注射不溶性气体(主要是全氟丙烷或六氟)也可用于封闭撕裂,而冷冻或光凝则用于封闭其边界。在气体被吸收后,玻璃体带将再次处于紧张状态,并出现复发的危险。另一方面,必须进入玻璃腔的事实本身也有一些风险。
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引用次数: 0
[Prevention of retinal detachment. Whom to treat?]. 预防视网膜脱离。治疗谁?
M Vallat, J Barthe, C Mathon, D Fritsch, F Van Coppenolle, J Detre, I Smolick

Natural history of retinal detachment (RD) studies on clinical exam of 200 patients revealed that RD, is the consequence of multiple risk factors preparing to PVD. This phenomenon depends therefore from peculiar background, patient's age, and opportunistic traumatism. The best prophylaxis would be represented by a mean of inducing PVD without retinal damage. Since no possibilities are present right now, retinopexy or surgical mechanical action are used as prophylactic methods. Results are discussed in this paper based on long-term-follow-up of 300 patients.

对200例视网膜脱离自然史(RD)患者的临床检查研究表明,RD是多种危险因素导致PVD的结果。因此,这种现象取决于特殊的背景、患者的年龄和机会性创伤。最好的预防方法是在不损害视网膜的情况下诱导PVD。由于目前不存在任何可能性,视网膜固定或手术机械作用被用作预防方法。本文通过对300例患者的长期随访,对结果进行了讨论。
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引用次数: 0
[Treatment of choroidal neovascularization in degenerative myopia]. 退行性近视脉络膜新生血管的治疗
A F Deutman, F Hendikse, C Hoyng

Choroidal neovascularization is quite frequent in degenerative myopia. If the neovascularization is near the center, a krypton laser photocoagulation can be effected. If they reach the center, no photocoagulation should be effected. We report here our results in the treatment by krypton laser and describe a simple technic for the determination of the exact position of the foveola, that can be displaced in degenerative myopia.

脉络膜新生血管在退行性近视中相当常见。如果新生血管在中心附近,氪激光可以进行光凝。如果它们到达中心,不应影响光凝。我们在这里报告了氪激光治疗的结果,并描述了一种简单的技术来确定退行性近视中可以移位的中央凹的确切位置。
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引用次数: 0
[Floppy eyelid syndrome. 5 cases]. 眼睑下垂综合症。5例)。
A Da Prá, M Brunzini, J O Croxatto, H Nano

First described in 1981, the floppy eyelid syndrome is characterized by loose upper lids that evert spontaneously and chronic papillary conjunctivitis. We present five patients with this syndrome and illustrate the distinctive clinical findings.

首次描述于1981年,松弛眼睑综合征的特点是上眼睑松散,自发和慢性乳头状结膜炎。我们提出了5例这种综合征的患者,并说明了其独特的临床表现。
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引用次数: 0
[Eye injuries due to pellet guns. Apropos of 7 cases]. [霰弹枪造成的眼部伤害。[7例]。
D Fournier, M Cherifi, A Salvanet-Bouccara, F Forestier, J Feys

The authors expose a series of seven cases of ocular trauma due to pellet guns. First, they describe the different kinds of lesions, their treatment, and their development. Then, they study the prognostic points, the mechanism of the secondary complications, and the therapeutic conduct to adopt in front of this type of perforating injuries with non-magnetic intraocular foreign body. They insist on the severity of this type of ocular trauma, and on the necessity of a modification of the law concerning pellet guns.

作者揭露了一系列的7例眼外伤的弹丸枪。首先,他们描述了不同类型的病变,它们的治疗方法,以及它们的发展。然后,研究该类非磁性眼内异物穿孔伤的预后要点、继发并发症的发生机制及治疗方法。他们坚持认为这类眼部创伤是严重的,并认为有必要修改有关霰弹枪的法律。
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引用次数: 0
[Familial agenesis of the lacrimal glands and ducts]. [家族性泪腺和泪管发育不全]。
S Auch-Roy-Mainguy, B Bordat, C Boudet

Authors report three cases of hereditary malformation of excretory lacrymal system, two children and their father. One of the two children have a lacrymal fistula. A surgical treatment was successful.

作者报告三例遗传性排泄性泪系统畸形,两个孩子和他们的父亲。其中一个孩子有泪道瘘管。手术治疗很成功。
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引用次数: 0
[Variations in the level of S antigen auto-antibodies and their relation to the development of retinitis pigmentosa (autosomal recessive genetic form)]. [S抗原自身抗体水平的变化及其与视网膜色素变性(常染色体隐性遗传形式)发展的关系]。
C D Heredia Garcia, P A Garcia Calderon

A group of 40 patients with retinitis pigmentosa (autosomal recessive) were studied. The levels of soluble retinal antigen (S antigen of human origin) auto-antibodies were measured by means of the enzyme-linked-immunosorbent assay. The results obtained were compared with those of a control population of 100 healthy subjects (p less than 0.001). A statistically significant correlation (r = 0.451, p less than 0.01) was observed when comparison was made between the anti-S levels and the time elapsed from the moment of retinitis pigmentosa diagnosis.

对40例视网膜色素变性(常染色体隐性遗传)患者进行了研究。采用酶联免疫吸附法测定视网膜可溶性抗原(人源性S抗原)自身抗体水平。将所得结果与100名健康受试者对照人群的结果进行比较(p < 0.001)。抗s水平与视网膜色素变性诊断时间的相关性有统计学意义(r = 0.451, p < 0.01)。
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引用次数: 0
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Ophtalmologie : organe de la Societe francaise d'ophtalmologie
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