儿童威尔逊病及其诊断的挑战:一个案例报告
1Pediatrics, Sree Balaji Medical College and Hospital, Chennai, IND.
Cureus
|September 2, 2024
概括
威尔逊病,是一种由ATP7B基因突变引起的铜代谢遗传性疾病,在一个12岁的男孩身上出现了神经和肝脏症状. 早期诊断和治疗对于管理这种罕见的神经代谢疾病至关重要.
科学领域:
- 遗传学 遗传学是一种遗传学.
- 神经学 神经学
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 威尔逊病是一种遗传性疾病,由于ATP7B基因突变,影响铜代谢.
- 它主要影响肝脏和大脑,导致铜积累.
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