Expert consensus on the genetic diagnosis for Dystrophinopathies / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 909-914, 2023.
Article
in Chinese
| WPRIM (Western Pacific)
| ID: wpr-1009233
Responsible library:
WPRO
ABSTRACT
Dystrophinopathies, including Duchenne muscular dystrophy, Becker muscular dystrophy and dilated cardiomyopathy, are X-linked recessive genetic disorders due to variants of the dystrophin gene, which can seriously affect quality of life and health. Genetic diagnosis plays a crucial role in their diagnosis, treatment, and prevention. How to rationally select and standardize the use of various genetic techniques is a skill that clinicians must acquire. By compiling expertise of experts from the relevant areas and guidelines published home and abroad, this consensus has provided a guidance from the perspective of genetic diagnosis for the selection of genetic techniques, testing strategies, and detection process for dystrophinopathies.
Full text:
Available
Database:
WPRIM (Western Pacific)
Main subject:
Quality of Life
/
Cardiomyopathy, Dilated
/
Dystrophin
/
Muscular Dystrophy, Duchenne
/
Consensus
/
Electrocardiography
Limits:
Humans
Language:
Chinese
Journal:
Chinese Journal of Medical Genetics
Year:
2023
Document type:
Article