Spinal muscular atrophy is an autosomal recessive disease. The severity of spinal muscular atrophy varies, and is the most common genetic cause of infant death.
She has a muscular atrophy.
muscular atrophy
Sven Brandt has written: 'Werdnig-Hoffmann's infantile progressive muscular atrophy' -- subject(s): Atrophy, Muscular, Diseases, In infancy and childhood, Infants, Muscular atrophy
The most common form of spinal muscular atrophy is childhood proximal SMA.
Diego Soto has written: 'Diego's story' -- subject(s): Muscular atrophy in children, Muscular atrophy
Bulbospinal muscular atrophy (Kennedy disease) manifests as muscle weakness between the ages of 20 and 40 years.
Muscular atrophy is a decrease in the mass of muscle. It can be a result of common diseases such as cancer, AIDS, renal failure and congestive heart failure. People who suffer from muscular atrophy have either partial or complete wasting away of the muscle, depending on the severity of the case.
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What is the diagnosis and treatment for muscular atrophy?
Muscular atrophy is when the muscles in the body begin to break down on a cellular level due to lack of oxygen, disease, or simply lack of excercise. Don't confuse it with necrosis. Necrosis is complete cell death. Atrophy is just a loss of muscular integrity (i.e. getting fat and losing strength).