先天性青光眼合并Hurler综合征和Lowe's综合征。临床和电子显微镜检查结果]。

S Lalive d'Epinay, C E Remé
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引用次数: 0

摘要

本文报告先天性青光眼合并一般代谢性疾病2例。1例患者表现为粘多糖增多症(赫勒综合征),另1例患者表现为洛氏眼-脑肾综合征。两例患者均行小梁切除术。用电子显微镜对切除组织进行分析。在这两种情况下,在小梁区和施勒姆管中都观察到明显的空泡或纤维状沉积物。这些改变可能是导致两名患者眼压升高的原因。
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[Congenital glaucoma in Hurler's syndrome and in Lowe's syndrome. Clinical and electron microscopy findings].

2 cases of congenital glaucoma combined with a general metabolic disease are described. 1 patient displayed the symptoms of a mucopolysaccharidosis (Hurler's syndrome), the other patient showed the characteristics of Lowe's oculo-cerebrorenal syndrome. In both patients a surgical trabeculectomy was performed. The excised tissues were analysed by electron microscopy. Distinct vacuolar or fibrillar deposits were observed in both cases in the trabecular region and in Schlemm's canal. Possibly, these alterations could have contributed to the raised intraocular pressure in both patients.

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