相关实验视频
Updated: May 5, 2026

A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
Published on: May 16, 2020
一个孩子的家族扩张性心肌病:一个病例报告
Ali Ismail1, Dima Khreis1, Amani Assaad1
1Department of Pediatric and Adolescent Medicine, American University of Beirut Medical Center, PO Box: 11-0236. Riad El Solh, Beirut, Beirut, 1107 2020, Lebanon.
儿童扩展性心肌病,通常与基因突变如肌光链3有关,具有心力衰竭和死亡的高风险. 目前的治疗重点是由于缺乏治愈疗法而改善预后.
科学领域:
- 儿童心脏病学 儿童心脏病学
- 遗传学 遗传学 是一个
- 心血管医学 心血管医学
背景情况:
- 扩张性心肌病 (DCM) 是儿童心力衰竭 (HF) 和心脏移植的主要原因.
- 诊断包括心电图,胸部X射线和心声回声图,但对儿科异常/家族DCM的治疗指南是有限的.
- 目前的儿科DCM管理侧重于改善预后,而不是提供治疗方法.
更多相关视频
08:42Cox-Maze IV Procedure Concomitant with Valvular Surgery In Situs Inversus Dextrocardia: A Single-Center Experience in China
Published on: February 11, 2022
03:45Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
相关概念视频
Myocarditis II: Clinical Features and Diagnostic Tests
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy V: Interprofessional Care