皮质性视力障碍(CVI):儿童渗透性脱髓鞘综合征的非典型表现

Najm Khan, R. Lakshmanan, Snehal Shah, L. Nagarajan
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引用次数: 0

摘要

渗透性脱髓鞘综合征(ODS)是一种独特的选择性脱髓鞘和大脑特定区域少突胶质细胞和星形胶质细胞破坏的过程,通常发生在渗透应激后几天。ODS最常被描述为与低钠血症的快速纠正有关,尽管它可能与其他电解质或代谢异常一起发生[10]。ODS在儿童中是相当罕见的疾病[2,3],包括脑桥中央和脑桥外髓鞘溶解。ODS可能与共济失调、球功能障碍、步态障碍、痉挛、癫痫、脑病甚至昏迷和死亡等形式的神经损伤有关。它可能导致长期的神经发育后遗症[2,3]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cortical Visual Impairment (CVI): An Atypical Manifestation of Osmotic Demyelination Syndrome in a Child
Osmotic Demyelination Syndrome (ODS) is a unique process of selective demyelination and destruction of oligodendrocytes and astrocytes in specific areas of the brain that usually occurs a few days after an osmotic stress [1]. ODS has been described most frequently in association with a rapid correction of hyponatremia, though it may occur with other electrolyte or metabolic abnormalities [1]. ODS is a rather uncommon disorder in childhood [2,3] and encompasses central pontine and extra pontine myelinolysis. ODS may be associated with neurological impairment in the form of ataxia, bulbar dysfunction, gait disturbances, spasticity, seizures, encephalopathy and even coma and death. It may result in long term neurodevelopmental sequelae [2,3].
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