Accepting that you or a family member has BMD is hard. To compensate for weakening muscles, a person with BMD may walk with a waddling gait, walk on his toes, or stick out his abdomen. See the Medical Management section for more information on managing heart problems in BMD. In its most … Key points about Becker muscular dystrophy in children. Early symptoms include: a waddling gait; Becker muscular dystrophy signs and symptoms show up in patients during their teens or young adult years. There also is some weakness of arm and neck muscles. At Another Johns Hopkins Member Hospital: Becker muscular dystrophy is similar to Duchenne muscular dystrophy and is characterized by progressive muscle weakness. Becker muscular dystrophy is similar to Duchenne muscular dystrophy, but it’s less severe. But Becker muscular dystrophy starts later -- … Limb-girdle. Muscular dystrophy (MD) is a group of muscle diseases that results in increasing weakening and breakdown of skeletal muscles over time. To compensate for weakening muscles, a person with BMD may walk with a waddling gait, walk on his toes, or stick out his abdomen. Like muscles in the limbs, heart muscles also can be weakened by lack of dystrophin. Muscle weakness occurs primarily in your arms and legs, with symptoms appearing in between age 11 and 25. You may also want to join a muscular dystrophy support group. This type of muscular dystrophy likewise more typically impacts young boys, according to iytmed.com. Becker Muscular Dystrophy. Males are primarily affected by this disease, and the onset usually occurs between ages five and 15. Orthopaedic surgeons with expertise in muscular dystrophy can treat contractures and scoliosis. The age of onset varies as well. Although girls can be carriers and mildly affected, it's much more common in boys. However, Becker muscular dystrophy is less common than Duchenne muscular dystrophy and is associated with milder clinical symptoms. Muscular dystrophies are a group of genetic conditions characterized by progressive muscle weakness and wasting (atrophy). Becker muscular dystrophy (BMD) is an inherited condition that causes progressive weakness and wasting of the skeletal and cardiac (heart) muscles. It causes muscles to weaken and waste over time, leading to increasing and often severe disability. All four of the heart’s chambers are involved in fibrosis, and heart failure can rapidly progress.4,5. Muscle biopsy: For those children who have clinical evidence of Duchenne muscular dsytrophy but who do not show one of the common mutations, a small sample of muscle tissue is taken and examined under a microscope to confirm the diagnosis. Becker muscular dystrophy symptoms. Becker muscular dystrophy (BMD) is an inherited degenerative muscle disease. Becker muscular dystrophy affects the muscles of the hips, pelvic area, thighs and shoulders, as well as the heart.Becker muscular dystrophy (BMD) is one of nine types of muscular dystrophy, a group of genetic, degenerative diseases primarily affecting voluntary muscles. The symptoms of Becker muscular dystrophy are similar but tend start in the mid-twenties or later, are milder, and progress more slowly. What are the symptoms of Becker muscular dystrophy? The condition is named for the German physician Peter Emil Becker, who first described this variant of muscular dystrophy in the 1950s. The symptoms usually occur in childhood by 11 years of age. Becker muscular dystrophy (BMD) is a rare inherited disorder of the muscles. But the disease rarely causes health problems until a child has muscle weakness in the hips and pelvis. Becker dystrophy has later onset and causes milder symptoms. Signs and Symptoms The pattern of muscle loss in BMD usually begins with the hips and pelvic area, the thighs, and the shoulders. The age of onset and rate of progression can vary. Respiratory muscles often stay strong in BMD for many years, but eventually, they may become weaker than is optimal for breathing and coughing (to clear secretions from the respiratory tract). A doctor may prescribe steroid medications to help individuals remain able to walk for as long as possible. Myotonic Muscular Dystrophy This form of muscular dystrophy starts with muscle weakness in the face and then moves on to the feet and hands. Because muscular dystrophy doesn’t affect nerves directly, touch and other senses remain normal, as does control over the smooth, or involuntary, muscles of the bladder and bowel, and sexual functions. Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked recessive disorders caused by mutations in the dystrophin gene. Doctors believe that dystrophin abnormalities in the brain may cause cognitive and behavioral deficits and other neuropsychiatric disturbances.6 Intellectual disability or cognitive impairment are not common or severe in patients diagnosed with BMD in comparison to those diagnosed with DMD. The main sign of muscular dystrophy is progressive muscle weakness. Stay informed. This type of muscular dystrophy likewise more typically impacts young boys, according to iytmed.com. Symptoms of Becker muscular dystrophy The rate of muscle degeneration in people with Becker muscular dystrophy (BMD) varies greatly between individuals. 2021, Muscular Dystrophy Association Inc. All rights reserved. Symptoms of Becker muscular dystrophy. Duchenne muscular dystrophy is similar to this disease, but BMD tends to have a later onset and slower progression. Some people may require a wheelchair by the time they reach their 30s; others may be able to continue walking with or without a cane for many years. The majority of the female carriers do not have any sign of the condition at all, while a small number of carriers may have a muscular dystrophy that is almost as severe as boys with Duchenne muscular dystrophy. Other extremely rare forms of muscular dystrophy can affect both girls and boys. Some types are also associated with problems in other organs. Becker muscular dystrophy is a life-changing disease for you and your family. Becker MD symptoms can range from mild to almost as severe as the symptoms of Duchenne MD. In some cases, Becker muscular dystrophy can lead to life-threatening health problems, as heart and breathing muscles weaken. As muscles weaken, patients may notice changes when they participate in physical activities and sports. Becker muscular dystrophy causes similar symptoms as DMD, with a couple of typical differences: Later onset of symptoms (twenties and thirties) Muscle weakness starts … not be able to walk quickly, run smoothly, or maintain a running pace. Diagnosis is suggested clinically and is confirmed by genetic testing or analysis of the protein product (dystrophin) of the mutated gene. Talk to your caregivers, family, or friends about your feelings. Eye problems can vary based on the type of muscular dystrophy. It worsens at a much slower rate. Symptoms may appear as late as age 25. Leg muscles become increasingly weaker. Becker muscular dystrophy is an X-linked recessive inherited disorder characterized by slowly progressing muscle weakness of the legs and pelvis. Chronic respiratory symptoms, before they present cardiac symptoms the presence of creatine kinase, an enzyme that when! And echocardiograms 5-24 has Duchenne and Becker forms of muscular dystrophy is similar to those of Duchenne muscular is! Kids do of Use | State Fundraising Notices tests: genetic Blood tests: Blood! And is confirmed by genetic testing or analysis of the protein dystrophin clinically and is characterized progressive! 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