Nöroakantositozis: Olgu sunumu

Turan Poyraz, A. Çiftçi, Ö. Akgün, Serap Kasa, E. İdiman
{"title":"Nöroakantositozis: Olgu sunumu","authors":"Turan Poyraz, A. Çiftçi, Ö. Akgün, Serap Kasa, E. İdiman","doi":"10.5350/BTDMJB.20141103092408","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":321087,"journal":{"name":"Medical journal of Bakirköy","volume":"23 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2017-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical journal of Bakirköy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5350/BTDMJB.20141103092408","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

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.
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信