Duchenne muscular dystrophy
Duchenne muscular dystrophy is the genetic disorder that causes progressive muscle degeneration and weakness, typically affecting boys in early childhood and leading to mobility challenges by young adulthood. It is caused by a mutation in the gene responsible for producing dystrophin, a protein needed for muscle strength and integrity. Treatment focuses on managing symptoms and maintaining quality of life.
marked by severe muscle weakness from birth, with infants displaying "floppiness" and very little voluntary movement. Nonetheless, a child with CMD may learn to walk, either with or without some assistive device, and live into young adulthood or beyond
Muscular dystrophy is one. It is typically an inherited disorder that causes degeneration of the skeletal muscles.
Muscular dystrophy
Muscular dystrophies are a group of genetic muscle disorders that cause progressive weakness and degeneration of the skeletal muscles without affecting the nervous system. Duchenne muscular dystrophy is an example of a muscular dystrophy that fits this description.
Muscular sclerosis is hardening and degeneration of the myelin sheath. Muscular sclerosis Multiple sclerosis is a disorder marked by destruction of the myelin sheath on neurons in the CNS and replacement with hard scar tissue.
yea bcuz muscular dystrophy is the name of the disease and therefore is a proper noun
Spinal muscular atrophies (SMAs) are a wide group of genetic disorders characterized by primary degeneration of anterior horn cells of the spinal cord, resulting in progressive muscle weakness.
muscular dystrophy
Yes, hypotonia can be related to muscular dystrophy. Muscular dystrophy encompasses a group of genetic disorders characterized by progressive muscle weakness and degeneration, often leading to hypotonia, especially in young children. The degree of hypotonia may vary depending on the specific type of muscular dystrophy and its progression. However, hypotonia can also result from other conditions unrelated to muscular dystrophy.
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 old, rotten food gave the hunger soldiers a bad case of dystrophy.