seems to be the same according to weblink,p://puneataxiasupport.wordpress.com/types-of-ataxia-muscular-dystrophy/ Ramajayam
Muscular dystrophy is a group of genetic disorders characterized by muscle weakening and wasting, while Duchenne muscular dystrophy (DMD) is a specific type of muscular dystrophy caused by mutations in the dystrophin gene. DMD is the most common and severe form of muscular dystrophy, typically affecting boys and leading to progressive muscle weakness and loss of function.
I believe you are referring to muscular dystrophy, this is a inherited degenerative muscular disease, and can only be inherited from parents.There are a number of types of muscular dystrophy but this along with all other inherited diseases are not infections.
Muscular dystrophy is a genetic disorder that causes progressive weakening and deterioration of the muscles. It results from mutations in genes responsible for the structure and function of muscle fibers. There are several types of muscular dystrophy, each with specific genetic causes and patterns of muscle weakness.
Muscular dystrophy is a genetic condition caused by mutations in genes responsible for the structure and function of muscles. These mutations lead to muscle weakness, wasting, and degeneration over time. There are many different types of muscular dystrophy, each caused by mutations in specific genes.
The main types include congenital myopathy, muscular dystrophy , inflammatory myopathy, and drug-induced myopathy.
Muscular dystrophy (MD) encompasses a group of genetic disorders that lead to progressive muscle weakness and degeneration. The most common form, Duchenne muscular dystrophy (DMD), affects approximately 1 in 3,500 male births. Other types of muscular dystrophy have varying prevalence rates, but overall, MD collectively affects about 1 in 5,000 to 1 in 10,000 individuals. The exact frequency can vary based on the specific type and population studied.
Some types of muscular dystrophy involve pathologic fat deposits within the muscle tissue.
Two types of muscular diseases are muscle dystrophy and spinal muscle attrophy. Both are genetic, though.
There are many types of MD. If the diagnosis is Duchennes MD, death usually occurs in the late teens, early twenties.
The short answer is yes, absolutely. You may be primarily thinking of sex-linked dystrophies, such as Duchenne's or Becker's Muscular Dystrophy. The gene mutations for these types of dystrophy are recessive traits located on the X chromosome. It is vastly more common in boys then in girls because boys only have one X chromosome. If they get the gene for these dystrophies on their mom's X chromosome, then they will not have another X chromosome to "mask" the trait, and thus they will get the disease. Since girls have two X chromosomes, this is a lot rarer. Even if one X chromosome has the gene for the disease, as long as the other one doesn't, they are only a carrier, they don't actually have symptoms. There are only two ways where a girl can get a sex-linked dystrophy: if her mom is a carrier and her dad has the disease, or if her X chromosomes mutate in a way that make her have the gene on both X chromosomes. However: Muscular dystrophies come in dozens of types. Sex linked varieties may be among the most common, but there are plenty out there that are autosomal (i.e.: not sex-linked). Some come from autosomal recessive genes, other come from spontaneous mutations. For those types of muscular dystrophy, girls are just as likely to get them as boys.
MD is a genetic disorders in which strength and muscle bulk slowly weakens. It is caused by incorrect or missing genetic information. Without this information you can not build or maintain healthy muscles. You slowly lose the ability to walk or even sit up right. This disease can occur at any age in a persons life and there is no known cure.