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Glaucoma With the Oculocerebrorenal Syndrome of Lowe.

机译:青光眼与劳氏眼脑肾综合征。

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PURPOSE:: To further describe the glaucoma with the oculocerebrorenal syndrome of Lowe (OCRL) including the responsible filtration angle abnormalities and response to treatment. METHODS:: The scientific literature regarding the glaucoma associated with OCRL from 1952, when the first report of the syndrome appeared, to the present was reviewed. The medical records of 7 patients with OCRL were studied. The occurrence of glaucoma, corneal changes secondary to glaucoma, gonioscopic abnormalities, iris features, and response to glaucoma surgery were recorded. RESULTS:: Signs of glaucoma are defining abnormalities leading to recognition of OCRL. The OCRL medical literature reports the frequency of glaucoma, secondary clinical signs of increased intraocular pressure (IOP), and results of glaucoma surgery, but little information related to the responsible filtration angle abnormalities. Glaucoma was present in 71% (5 of 7) of patients studied, and was recognized in infancy in 9 of their 10 eyes. Gonioscopy wasperformed in 6 OCRL patients and revealed the constant presence of open angles, primary filtration angle anomalies, and defects considered secondary to previous infantile lens extractions. The observed anomalies were anterior insertion of the iris, narrowing of the ciliary body band, and decreased visibility of the scleral spur. The angle defects felt to be acquired following lens surgery included a more anterior insertion of the iris on to the trabecular meshwork, pigment dusting of the angle tissues, and iris synechial abnormalities related to the surgery. Bilateral goniotomies were unsuccessful in 4 of 4 patients. The fundi of 6 of 7 patients showed normal optic disc development with variable abnormalities secondary to glaucoma, and normal retinal vessels. Minimal evidence of macular development was observed in a single patient from 1 month of age to his most recent examination at 14 months of age. CONCLUSION:: A primary X-linked infantile glaucoma is a defining and frequent component of OCRL and is secondary to expression of a primary filtration angle anomaly. Goniotomy was unsuccessful in all (8) operated eyes. The adverse effects of cataract surgery on the filtration angle structures may influence the results of goniotomy surgery by superimposing a secondary aphakic glaucoma component that may explain the need for alternative glaucoma surgery.
机译:目的::进一步描述患有劳氏眼脑肾综合征(OCRL)的青光眼,包括负责的滤过角度异常和对治疗的反应。方法:回顾了自1952年首次出现该综合征的青光眼与OCRL相关的科学文献。研究了7例OCRL患者的病历。记录青光眼的发生,继发于青光眼的角膜变化,眼底镜异常,虹膜特征和对青光眼手术的反应。结果:青光眼的迹象定义了导致OCRL识别的异常。 OCRL医学文献报道了青光眼的发生率,眼内压(IOP)升高的继发临床体征以及青光眼手术的结果,但有关负责的滤过角异常的信息很少。青光眼出现在研究的患者中的71%(7个中的5个),并且在10眼中有9眼被识别为婴儿期。在6例OCRL患者中进行了角膜镜检查,结果发现持续存在开角,主要滤过角异常以及以前的婴儿晶状体摘除术后继发的缺陷。观察到的异常是虹膜的前部插入,睫状体带变窄以及巩膜骨刺的可见性降低。晶状体手术后感觉到的角缺损包括虹膜更早地插入小梁网,角组织的色素沉积以及与手术有关的虹膜联合异常。 4名患者中有4名双侧切角术未成功。 7名患者中有6名的眼底显示出正常的视盘发育,继发于青光眼的可变异常异常和正常的视网膜血管。从1个月大到14个月大的最新检查中,只有一名患者观察到了黄斑发育的最小证据。结论:原发性X连锁婴儿型青光眼是OCRL的定义和常见组成部分,其次于原发性滤过角异常的表达。所有(8)手术的眼睛均未进行切角手术。白内障手术对滤过角结构的不利影响可能会叠加二次无晶状体青光眼组件,从而可能影响角膜切开术的结果,这可能解释了替代性青光眼手术的必要性。

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