种系GATA2缺乏的神经学表现:附2例报告

Alastair K. Williams, Ryan J. Stubbins, Eric McGinnis, John A. Maguire, Persia Pourshahnazari, Claudie Roy, Luke Y.C. Chen, Thomas J. Nevill
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引用次数: 0

摘要

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