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Some diseases that result from inherited changes in DNA sequence include cystic fibrosis, sickle cell anemia, Huntington's disease, and Duchenne muscular dystrophy. These diseases are caused by mutations in specific genes that can be passed from parents to their offspring.
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.
muscular dystrophy poliomyelitis muscular sclerosis
muscular dystrophy
muscle aches? Per a physician, they indicated muscular dystrophy which includes over 100 forms of the muscular dystrophy.
1. Cystic Fibrosis 2. Huntington's Disease 3. Down Syndrome 4. Duchenne Muscular Dystrophy 5. Sickle Cell Anemia 6. Celiac Disease 7. Becker Muscular Dystrophy 8. Noonan Syndrome 9. Thalassemias 10. Bloom's Syndrome
The missing molecule in Duchenne muscular dystrophy is dystrophin, which is a protein that helps maintain the structure and function of muscle cells. In individuals with Duchenne muscular dystrophy, mutations in the DMD gene lead to a deficiency or absence of dystrophin protein.
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 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.
In general diseases that attack the muscles are called myopathies. Muscular dystrophy would be one example.
Muscular dytrophy is not spread it is heriditary.