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代谢性色素性视网膜病变:诊断与治疗尝试

Metabolic pigmentary retinopathies: diagnosis and therapeutic attempts.

作者信息

Poll-The B T, Billette de Villemeur T, Abitbol M, Dufier J L, Saudubray J M

机构信息

Clinique et Unité de Recherche de Génétique Médicale, INSERM U12, Paris, France.

出版信息

Eur J Pediatr. 1992 Jan;151(1):2-11. doi: 10.1007/BF02073880.

Abstract

Retinal degeneration in children occurs in errors of lipid, peroxisomal and mitochondrial (including respiratory chain) metabolism. In this review the most frequent inborn errors of metabolism with retinal degeneration are discussed including abetalipoproteinaemia, classical Refsum disease, neuronal ceroid lipofuscinosis, hydroxydicarboxylic aciduria, Sjögren-Larsson syndrome, infantile Refsum disease, Kearns-Sayre syndrome and gyrate atrophy. These metabolic disorders must be differentiated from those with retinal degeneration but without known metabolic basis. In patients with such a disorder metabolic investigations should be considered whenever atypical manifestations are encountered.

摘要

儿童视网膜变性发生于脂质、过氧化物酶体和线粒体(包括呼吸链)代谢异常。本文综述了伴有视网膜变性的最常见先天性代谢异常,包括无β脂蛋白血症、经典型Refsum病、神经元蜡样脂褐质沉积症、羟基二羧酸尿症、舍格伦-拉尔森综合征、婴儿型Refsum病、卡恩斯-塞尔综合征和回旋状萎缩。这些代谢紊乱必须与那些伴有视网膜变性但无已知代谢基础的疾病相鉴别。对于患有此类疾病的患者,一旦遇到非典型表现,就应考虑进行代谢检查。

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