神经元类脂褐细胞病

Ceroid Lipofuscinoses
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摘要

儿童神经退行性疾病,发病率约为1 / 25,000。根据发病年龄、临床特征、生化分析和患者组织电镜详细病理检查,将本病分为几种亚型。ncl的特点是进行性运动和认知功能减退、癫痫发作、早期死亡,并经常出现视力丧失。神经元类脂褐变
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuronal Ceroid Lipofuscinoses
neurodegenerative disorders of childhood, with an incidence of about 1 in 25,000 births. Several subtypes of the disease are classified on the basis of age of onset, clinical features, biochemical analysis and detailed pathological examination of patient tissue with electron microscopy. NCLs are characterized by progressive motor and cognitive deterioration, seizures, early death, and often visual loss. NEURONAL CEROID LIPOFUSCINOSES
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