Neurologic Manifestations of Germline GATA2 Deficiency: A Report of Two Cases

Alastair K. Williams, Ryan J. Stubbins, Eric McGinnis, John A. Maguire, Persia Pourshahnazari, Claudie Roy, Luke Y.C. Chen, Thomas J. Nevill
{"title":"Neurologic Manifestations of Germline <i>GATA2</i> Deficiency: A Report of Two Cases","authors":"Alastair K. Williams, Ryan J. Stubbins, Eric McGinnis, John A. Maguire, Persia Pourshahnazari, Claudie Roy, Luke Y.C. Chen, Thomas J. Nevill","doi":"10.7326/aimcc.2022.1087","DOIUrl":null,"url":null,"abstract":"Germline pathogenic mutations in the GATA2 gene, a critical transcription factor in hematopoietic and neurologic development, are known to cause various syndromes characterized by both hematopoietic (for example, monocytopenia, myelodysplastic syndrome) and extra-hematopoietic (for example, lymphedema, atypical and mycobacterial infections) manifestations. Neurologic features of this disease need to be better understood. We describe 2 patients with germline GATA2 deficiency who developed a progressive neurologic illness characterized by upper motor neuron weakness, bulbar and cerebellar dysfunction, pronounced white matter magnetic resonance imaging abnormalities, and noninfectious leukoencephalopathy with cerebellar degeneration. These neurologic findings may be a novel extra-hematopoietic manifestation of germline GATA2 deficiency.","PeriodicalId":72222,"journal":{"name":"Annals of internal medicine. Clinical cases","volume":"7 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of internal medicine. Clinical cases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7326/aimcc.2022.1087","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

Germline pathogenic mutations in the GATA2 gene, a critical transcription factor in hematopoietic and neurologic development, are known to cause various syndromes characterized by both hematopoietic (for example, monocytopenia, myelodysplastic syndrome) and extra-hematopoietic (for example, lymphedema, atypical and mycobacterial infections) manifestations. Neurologic features of this disease need to be better understood. We describe 2 patients with germline GATA2 deficiency who developed a progressive neurologic illness characterized by upper motor neuron weakness, bulbar and cerebellar dysfunction, pronounced white matter magnetic resonance imaging abnormalities, and noninfectious leukoencephalopathy with cerebellar degeneration. These neurologic findings may be a novel extra-hematopoietic manifestation of germline GATA2 deficiency.
种系GATA2缺乏的神经学表现:附2例报告
GATA2基因是造血和神经发育的关键转录因子,其种系致病性突变已知可引起以造血(例如单核细胞减少症、骨髓增生异常综合征)和造血外(例如淋巴水肿、非典型和分枝杆菌感染)表现为特征的各种综合征。这种疾病的神经学特征需要更好地了解。我们描述了2例种系GATA2缺乏的患者,他们发展为进行性神经系统疾病,其特征是上运动神经元无力,球和小脑功能障碍,明显的白质磁共振成像异常,以及非传染性白质脑病伴小脑变性。这些神经学上的发现可能是种系GATA2缺乏的一种新的造血外表现。
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
CiteScore
0.10
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