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Exploring the diagnostic journey of individuals and families with mitochondrial disease

探索患有线粒体疾病的个人和家庭的诊断之旅

批准号：

449398

负责人：

Vas Maria

金额：

$1.27万

依托单位：

University of Manitoba

依托单位国家：

加拿大

项目类别：

Studentship Programs

财政年份：

2020

资助国家：

加拿大

项目状态：

已结题

起止时间：

2020-12-01 至 2021-12-01

来源：

https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=449398&lang=en

关键词：

Diagnostic Odyssey Genetic Counselling Genetics Health Services Research Metabolic Diseases Mitochondrial Disease Patient Support

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英文摘要

Mitochondrial diseases are a complex group of inherited metabolic disorders that affect 1 in 5000 people. Diagnosis of mitochondrial disease (MID) is complicated and typically involves visits with various specialists, undergoing many tests, and often bein

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