Muscular Dystrophies
Overview
Muscular dystrophy (MD) is a group of muscle diseases that weaken the musculoskeletal system and affect a person’s ability to walk. These are genetic conditions and can be inherited, or an individual may be the first one in their family affected.
Muscular dystrophies are characterised by progressive skeletal muscle weakness, defects in muscle proteins, and the death of muscle cells and tissue. There are several defined types of MD, which are diagnosed based on the specific presentation of muscle weakness. These can now generally be confirmed by gene tests for the specific genetic fault, where an error in a gene is what is causing the pattern of weakness.
For more information on each type, please select from the A-Z Directory.
If you have any questions, please email them to info@mda.org.nz, and we will endeavour to answer them as quickly as possible for you.