Becker muscular dystrophy
Other Names for this Disease
- Benign pseudohypertrophic muscular dystrophy
- Becker's muscular dystrophy
- Muscular dystrophy, Becker type
- Muscular dystrophy pseudohypertrophic progressive, Becker type
- Becker dystrophinopathy
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.
Tests & Diagnosis
Becker muscular dystrophy (BMD) may first be suspected in a person with signs or symptoms of BMD. Healthcare providers will often conduct neurological and muscle exams, as well as order specific laboratory tests. A careful medical history is also important to differentiate between BMD and Duchenne muscular dystrophy.
Exams in a person with BMD may reveal:
- Abnormally developed bones, leading to deformities of the chest and back (scoliosis)
- Abnormality of heart muscle function (cardiomyopathy)
- Congestive heart failure or irregular heartbeat (arrhythmias)
- Muscle deformities
- Contractures of heels and legs
- Fat and connective tissue (pseudohypertrophy) in calf muscles
- Muscle wasting that begins in the legs and pelvis, then progresses to the muscles of the shoulders, neck, arms, and respiratory system
Laboratory tests that help confirm the diagnosis include:
Last updated: 11/4/2015
- Kaneshiro NK, Hoch DB. Becker's muscular dystrophy. MedlinePlus. 2008; http://www.nlm.nih.gov/medlineplus/ency/article/000706.htm. Accessed 11/18/2009.
- The Genetic Testing Registry (GTR) provides information about the genetic tests for this condition. The intended audience for the GTR is health care providers and researchers. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.