沃尔夫拉姆综合征I型病例报告和综述-专注于早期诊断和遗传变异
Alexandru Daniel Jurca1, Larisa Bianca Galea-Holhos2, Aurora Alexandra Jurca3
1Department of Preclinical Disciplines, Faculty of Medicine and Pharmacy, University of Oradea, 410081 Oradea, Romania.
Medicina (Kaunas, Lithuania)
|July 27, 2024
概括
沃尔夫拉姆综合征1型是一种罕见的遗传疾病. 通过对WFS1基因变异进行遗传检测,早期诊断对于管理其严重,渐进的症状和改善患者结果至关重要.
科学领域:
- 遗传学 是一个遗传学.
- 神经科学是一个神经科学.
- 内分泌学 在内分泌学.
背景情况:
- 沃尔夫拉姆综合征1型是一种罕见的,自体相逆性神经退行性疾病.
- 它的特点是青少年糖尿病 (DM),视力缩 (OA),无味糖尿病 (DI) 和聋 (D) (DIDMOAD).
- 由WFS1基因的致病变体引起,导致预期寿命约为39年.
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