Turan Poyraz, A. Çiftçi, Ö. Akgün, Serap Kasa, E. İdiman
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引用次数: 0

摘要

神经棘细胞增多症是一种罕见的遗传性疾病。神经棘细胞增多症是一组罕见的与外周血涂片棘细胞增多症相关的神经退行性疾病。神经棘细胞增多症是一种皮层下型痴呆。神经棘细胞增多症患者可能经历额型人格改变(冷漠、易怒或冲动)。精神病、强迫症、焦虑和抑郁不太常见。在这个报告中,我们的目的是讨论一个延迟诊断的神经性棘细胞增多症病例与家族性神经学特征。
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Nöroakantositozis: Olgu sunumu
Neuroacanthocytosis: A case report Neuroacanthocytosis is a rare inherited disorder. Neuroacanthocytosis consists of a group of rare neurodegenerative disorders associated with acanthocytosis on the pheripheral blood smear. Neuroacanthocytosis is characterized by a subcortical type of dementia. Patients with neuroacanthocytosis may experience personality alterations of a frontal type (with apathy, irritability, or impulsiveness). Psychosis, obsessivecompulsive disorder, anxiety, and depression are less common. In this report, we aim to discuss a delayed diagnosed neuroacanthocytosis case with familial neurological features.
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