Do carriers of muscular dystrophy have symptoms?
Do carriers of muscular dystrophy have symptoms?
Carriers can have some symptoms of Duchenne, such as muscle weakness and heart problems. Though it is rare, some females can have the classic symptoms of Duchenne, and they are known as manifesting carriers. All carriers should be evaluated by a healthcare provider familiar with Duchenne.
How is Becker muscular dystrophy diagnosed?
The diagnosis of Becker muscular dystrophy is based on physical symptoms, family history, an elevated concentration of creatine kinase (CK) in the blood indicating destruction of muscle, and molecular genetic testing.
Does Becker muscular dystrophy cause pain?
Duchenne and Becker muscular dystrophy patients don’t tend to suffer from pain from their condition or loss of sensations, but they may experience cramps and general aching which can be treated with over-the-counter medications.
Can you get tested to see if you are a carrier for muscular dystrophy?
Carrier testing is done on a blood or saliva sample. There are different lab methods that can be used for carrier testing. The method for carrier testing should be determined by the woman’s family situation, including whether the mutation in the family is known and her family history.
What are the signs of Becker muscular dystrophy?
What Are the Signs & Symptoms of Becker Muscular Dystrophy?
- have more difficulty with sports.
- have trouble climbing stairs.
- not be able to walk quickly, run smoothly, or maintain a running pace.
- have trouble lifting heavy loads.
- have calf muscles that look bigger than normal, even though they’re weaker.
Who is most likely to get Becker muscular dystrophy?
Like Duchenne muscular dystrophy, Becker muscular dystrophy is a genetic condition that affects mostly males. Becker muscular dystrophy symptoms usually show up in a person’s teens or early adult years. Its course is slower than that of Duchenne’s and can be harder to predict.
Can a man with muscular dystrophy have children?
Carriers may not have any disease symptoms but can have a child with the mutation or the disease. DMD carriers are at risk for cardiomyopathy. Although DMD often runs in a family, it is possible for a family with no history of DMD to suddenly have a son with the disease.
