Heart muscle disease (cardiomyopathy ), occurs more commonly in BMD. Problems may include irregular heartbeats (arrhythmias ) and congestive heart failure. Symptoms may include fatigue, shortness of breath, chest pain, and dizziness
yea bcuz muscular dystrophy is the name of the disease and therefore is a proper noun
Elaine Myrtle Edwards Hutton has written: 'Duchenne muscular dystrophy' -- subject(s): Muscular dystrophy, Medical genetics
You can find pedigree diagrams for Muscular Dystrophy in scientific articles, textbooks on genetics, or on specialized websites that focus on genetic disorders or medical genetics. These diagrams visually represent the genetic relationships within families affected by Muscular Dystrophy.
Alternative NamesResources - muscular dystrophyInformationThe following organizations are good resources for information on muscular dystrophy:Muscular Dystrophy Association - www.mdausa.orgMuscular Dystrophy Family Foundation - www.mdff.org
There are many types of muscular dystrophy and are usually defined by where the symptons starts. Normal signs are soreness in the larger muscle groups, muscle weakness or poor balance ability. It's important to seek medical advise if you notice any signs of muscles weakness - such as problems with your balance capacity - on yourself or your child.
Yes, it is possible to die from MD (muscular dystrophy), although the condition itself is not directly fatal. Muscular dystrophy is a group of genetic disorders characterized by progressive muscle weakness and degeneration, which can lead to severe complications like respiratory failure, heart problems, or infections. The severity of these complications varies depending on the specific type of muscular dystrophy and the individual's overall health. Proper medical management can help mitigate risks and improve quality of life.
muscular problems
In most cases this is diagnosed by age five. In that case the child would need a wheelchair by about age 12. Most likely the child will start to have heart and lung issues by late teens or early twenties. My guess no longer than thirty.
you can break your muscle.
a careful medical history and a thorough physical exam to determine the distribution of symptoms and to rule out other causes. Family history may give important clues, since all the muscular dystrophies are genetic conditions
In the 1860s, descriptions of boys who grew progressively weaker, lost the ability to walk, and died at an early age became more prominent in medical journals. In the following ten years, French neurologist Guillaume Duchenne gave a comprehensive account of 13 boys with the most common and severe form of the disease (which now carries his name - Duchenne muscular dystrophy). It soon became evident that the disease had more than one form, and that these diseases affected males of all ages. Nine diseases including Duchenne, Becker, limb girdle, congenital, facioscapulohumeral, myotonic, oculopharyngeal, distal, and Emery-Dreifuss are always classified as muscular dystrophy.
Vascular Dystrophy