What Is Becker Muscular Dystrophy?
Source: Genetic and Rare Diseases (GARD) Information Center
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Becker Muscular Dystrophy
BMD; Becker MD
Becker muscular dystrophy (BMD) is an inherited condition that causes progressive weakness and wasting of the skeletal and cardiac (heart) muscles. It primarily affects males. BMD is a genetic form of muscular dystrophy. Learn more about causes, symptoms and treatment options.
Primary Myoblasts
Image by NIAMS/Photographer: Shuktika Nandkeolyar and Evelyn Ralston, Ph.D., NIAMS Light Imaging Section
Muscle Tissue: Cardiac Muscle
Image by Berkshire Community College Bioscience Image Library
Source: Genetic and Rare Diseases (GARD) Information Center
Drawing of boy with Duchenne muscular dystrophy
Image by Duchenne, Guillaume-Benjamin/Wikimedia
Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) can have the same symptoms and are caused by mutations in the same gene. BMD symptoms can begin later in life and be less severe than DMD. However, because these two kinds are very similar, they are often studied and referred to together (DBMD).
How many people are affected?
About 14 in 100,000 males 5 – 24 years of age
Who is more likely to be affected: males or females?
Males
When does muscle weakness typically begin?
DMD symptoms usually begin before 5 years of age. In BMD, symptoms usually appear later, even into adulthood.
Which parts of the body show weakness first?
Upper legs and upper arms
What other parts of the body can be affected?
Heart, lungs, throat, stomach, intestines, and spine
Source: Centers for Disease Control and Prevention (CDC)
Mutation
Image by National Human Genome Research Institute (NHGRI)
Source: Genetic and Rare Diseases (GARD) Information Center
X-linked recessive
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Source: Genetic and Rare Diseases (GARD) Information Center
Muscular Dystrophy - NICHD
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Source: Genetic and Rare Diseases (GARD) Information Center
Electromyography
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Source: Genetic and Rare Diseases (GARD) Information Center
physical therapy
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Source: Genetic and Rare Diseases (GARD) Information Center
Prognosis Icon
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Source: Genetic and Rare Diseases (GARD) Information Center
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