在呈现遗传确认的沃尔夫拉姆综合征的神经眼科变异性:一个案例系列和审查
Ruben Jauregui1, Nicolas J Abreu1, Shani Golan2
1Department of Neurology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Brain sciences
|July 29, 2023
概括
沃尔夫拉姆综合征是一种罕见的神经退行性疾病,表现出超出经典表型的多种症状. 早期诊断对于管理这种遗传疾病至关重要,即使是异常表现.
科学领域:
- 遗传学 遗传学 是一个
- 神经学 神经学
- 眼科医生 眼科 眼科
背景情况:
- 沃尔夫拉姆综合征是一种罕见的神经退行性疾病,与WFS1或CISD2基因突变有关.
- 经典的表型包括视力缩,糖尿病1型,无味糖尿病和聋.
- 然而,沃尔夫拉姆综合征表现出显著的表型异质性,临床表现和发病年龄各不相同.
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