[在治疗法布里病时得到了什么证实?]
1Allgemeine Innere Medizin D sowie Nieren- und Hochdruckkrankheiten und Rheumatologie, Interdisziplinäres Fabry Zentrum (IFAZ), Universitätsklinikum Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Deutschland.
Innere Medizin (Heidelberg, Germany)
|August 6, 2024
概括
费布里病是一种罕见的遗传性疾病,由低α-银酸酶A活性引起. 目前的治疗方法包括酶替代和陪伴疗法,正在研究新的选择.
科学领域:
- 遗传学和罕见疾病.
- 溶酶体储存障碍 溶酶体储存障碍
- 代谢性疾病是一种代谢性疾病.
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