对于法布里病治疗的临床特征和最近的进展
1Developmental Metabolic Neurology Branch, National Institute of Neurological Disorders and Stroke, Bldg 10, Room 3D03, National Institutes of Health, 10 Center Dr, MSC 1260, Bethesda, MD 20892-1260, USA.
弗拉布里病是一种溶酶体储存障碍,由于α-银酸酶A缺乏,导致严重的器官损伤. 用静脉注射的α-galactosidase A进行酶替代疗法对患者来说是安全有效的.
科学领域:
- 生物化学 生物化学
- 遗传学 是一个遗传学.
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 费布里病是一种X关联的衰退性 lysosomal 储存障碍,由α-galactosidase A 缺乏引起.
- 这种缺乏导致全球三基胺的积累,导致渐进的多器官功能障碍和早期死亡.
- 虽然主要影响男性,但女性携带者可以表现出显著的临床表现,包括中风风险.
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