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Becker muscular dystrophy primarily affects boys and men.3 Early diagnosis of Becker muscular dystrophy can aid in preserving muscle function and symptom management.4 Begin the diagnosis process by scheduling an appointment with your Primary Care physician or Neurologist to learn more.
Becker muscular dystrophy diagnosis begins with a physical examination after initial symptoms appear.9
Elevated Creatine Kinase (CK) plasma level guides toward a potential diagnosis of Becker muscular dystrophy.11 Individuals living with Becker muscular dystrophy may have up to 50 times the normal CK level.1
Diagnosis is confirmed with genetic testing which identifies the underlying mutation.10
Becker muscular dystrophy and Duchenne muscular dystrophy (DMD) are caused by a mutation on the dystrophin gene; both diseases may share symptoms and Becker may be initially diagnosed as Duchenne. Additionally, because Becker is a typically progressive disease affecting muscles, it may be confused with limb-girdle muscular dystrophy (LGMD).1 It is important to work with your Care Team to receive an accurate diagnosis and begin proactively managing your condition to preserve muscle function.
“Being proactive in the management of your Becker muscular dystrophy is very important as it's a progressive disorder. The earlier you act, the more you may be able to minimize your symptoms and mitigate the challenges that may arise.”
Charlie – Living with Becker
Muscle weakness is a key symptom of Becker muscular dystrophy.1 Muscles in your body support functions critical to independent living, such as walking, getting dressed and going to the bathroom.
When symptoms of Becker start, individuals living with Becker complain of muscle cramps and pain with strenuous physical activity.11
Walking problems are usually noticed by age 15.3 Muscle function loss is irreversible.4
Since the heart is made of muscle, Becker muscular dystrophy can cause weakening of the heart. This may lead to heartbeat irregularities and the heart not pumping blood as well as it should in a condition called dilated cardiomyopathy.5 Dilated cardiomyopathy is a serious heart condition requiring cardiologist care. In some cases, dilated cardiomyopathy may be the first sign of Becker muscular dystrophy.5
Becker can cause endocrine related symptoms including low levels of testosterone.13 Low testosterone levels can limit muscle development and affect reproductive function.
Gastrointestinal symptoms including trouble swallowing, constipation, reflux, bloating, and stomach discomfort can be seen in individuals living with Becker muscular dystrophy3 and can be managed with the help of a Gastroenterologist or Primary Care physician.
Muscle weakness caused by Becker muscular dystrophy can also affect the respiratory system. The diaphragm and other respiratory muscles can weaken resulting in difficulties breathing.6 If this happens, individuals with Becker can work with a respiratory specialist to test their breathing function. Medical equipment to support breathing may be needed as the condition progresses.
Becker muscular dystrophy can contribute to developmental and motor delays. Learning disability and behavioral issues may also be symptoms of Becker.12 Individuals living with Becker can consider consulting with a Neurologist to coordinate an individual treatment plan.
Communicate any changes in muscle function and mobility to your Care Team. An open dialog can help guide your Care Team to improve your current Becker management plan.