The mutations mean that the cells that should maintain your muscles can no longer fulfil this role leading. In most cases muscular dystrophy MD runs in families.
Myotonic Muscular Dystrophy Symptoms Causes Diagnosis Treatment And Coping
The causes are genetic.
What causes muscular dystrophy. There are more than 30 types of muscular dystrophy that result in muscle weakness. The symptoms and causes are. 10 rows Muscular dystrophy is a group of inherited diseases characterized by weakness and wasting.
1 There are three different inheritance patterns for most forms of MD. Muscular dystrophy is caused by genetic mutations that interfere with the production of muscle proteins that are needed to build and maintain healthy muscles. It occurs due to a mutation in the gene for a muscle protein called dystrophin.
It usually develops after inheriting a faulty gene from one or both parents. These spontaneous mutations can then be inherited by an affected persons offspring. It is the second most common form of muscular dystrophy and affects the hip thigh and shoulder muscles.
DMD is the most common form of muscular dystrophy. Most cases of MD are caused by gene mutations changes in the DNA sequence that affect muscle proteins. Becker muscular dystrophy BMD a milder form of muscular dystrophy is also caused by DNA variants in the DMD gene.
Over time the muscles get weaker disturbing the gait a persons manner of walking and the ability to perform daily activities. While there is no known cure for DMD there are treatments that can help control symptoms. The same gene which is responsible for Duchenne muscular dystrophy is the reason for the present genetic condition.
Although most forms of muscular dystrophy are caused by a mutation on the X chromosome influencing production of a protein called dystrophin a protein needed to. This damage and weakness is due to the lack. Muscular dystrophy causes are attributed to defects in specific genes that code for muscle proteins.
To get an insight on what causes muscular dystrophy keep reading this article. Muscular dystrophy abbreviated as MD is an umbrella term for a group of muscle related ailments. Muscular dystrophy is a group of inherited diseases that damage and weaken your muscles over time.
Therefore the sign symptoms inheritance pattern chromosomal location and causes are the same as the above condition. Mutation in genes responsible for healthy muscle structure and function causes muscular dystrophy. This genetic disease may be inherited from one or both parents.
This mutation means that the cells responsible for maintaining the muscle will no longer do their job which will lead to muscle weakness and disability in the person. Muscular dystrophies are a group of genetic diseases causing progressive weakness and loss of muscle mass. There are a few conditions that can develop and cause muscular dystrophy.
The mutations are usually inherited but in some cases they occur spontaneously. MD is caused by mutations alterations in the genes responsible for healthy muscle structure and function.