疑似线粒体功能障碍和复杂的病理生理学在致命的高移动埃勒斯-丹洛斯综合征:从病例报告和尸检结果的见解
Arash Shirvani1, Purusha Shirvani1, Ugochukwu Jonah2
1Ehlers-Danlos Syndrome Clinical Research Program, Section of Endocrinology, Diabetes, Nutrition and Weight Management, Department of Medicine, Boston University Chobanian & Avedisian School of Medicine, Boston, MA 02118, USA.
超移动埃勒斯-丹洛斯综合征 (hEDS) 可能涉及线粒体功能障碍,正如一个患有高级hEDS的患者的案例研究所表明的那样. 需要进一步的研究来证实这种联系,并开发有针对性的疗法.
科学领域:
- 遗传学 遗传学 是一个
- 病理生理学 病理生理学
- 分子生物学分子生物学
背景情况:
- 超移动埃勒斯-丹洛斯综合征 (hEDS) 是一种复杂的多系统性结合组织疾病.
- 由于进展性并发症,它显著影响患者的生活质量.
更多相关视频
03:45Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
09:40Phosphorus-31 Magnetic Resonance Spectroscopy: A Tool for Measuring In Vivo Mitochondrial Oxidative Phosphorylation Capacity in Human Skeletal Muscle
Published on: January 19, 2017
相关概念视频
Mitochondrial Membranes
Electron Transport Chain: Complex I and II
ROS generation is regulated and maintained at moderate levels necessary...
Mitochondria
Lysosomal Hydrolases
Cross-bridge Cycle
