超越常态:威尔逊病和甲状腺功能低下症的不同寻常的共存
Rucha Sawant1, Pranav Chaudhari1, Khadija F Hamdulay2
1Internal Medicine, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research (DMIHER), Wardha, IND.
Cureus
|March 22, 2024
概括
威尔逊病是一种导致铜积聚的遗传性疾病,在一个患有神经和肝脏症状的年轻人身上表现异常. 这一案例突出了罕见的甲状腺功能低下症的共同发生,扩大了我们对威尔逊病表现的理解.
科学领域:
- 肝病学 肝病学是一种肝病学.
- 神经学 神经学
- 内分泌学 在内分泌学.
背景情况:
- 威尔逊病 (WD) 是一种遗传性疾病,其特点是器官中铜的过度积累,主要是肝脏和大脑.
- 它表现为广泛的临床症状,影响多个器官系统.
关键词:
过高酸盐血症的发生.低血症 (hypocalcaemia) 是一种低血症.甲状腺过敏症 (hypoparathyroidism) 是一种严重的疾病.完好无损的副甲状腺激素威尔逊病是威尔逊的疾病.更多相关视频
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