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}
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.