Want this question answered?
The most common form of spinal muscular atrophy is childhood proximal SMA.
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.
Spinal muscular atrophy (SMA) is a genetic disease that affects the motor neuron cells in the spinal cord. This would impact the person's ability to walk, eat, or breathe. Anything that is a genetic disease cannot be cured, however the symptoms can be minimized through treatment, surgery and/or medication.
Charles Norris discovered spinal muscular atrophy in 1958. While he was experimenting with lettuce, he noticed than SMN neurons flowing through the vegetable caused loss of motor function, which left the lettuce deformed.
cyctic fibrosis and spinal muscular atrophy(sma)
Destruction of the anterior horn of the spinal cord often results in muscular disorders. These include sclerosis, Charcotâ??Marieâ??Tooth disease, progressive muscular atrophy, and other muscular atrophies.
It is unlikely, but some babies with the proper care and a milder form of Spinal Muscular Atrophy type 1 can recover. Typically infants with SMA do not survive past 2 years of age.
Some of them do, but according to the website I found about it the African-American population is one of the least-likely to get it.
John Bradford Goodman died on April 9, 2008, in Austin, Texas, USA of complications from spinal muscular atrophy.
SMA = Spinal muscular atrophy. There are different types of SMA, all I believe are genetic and are autosomal recessive. They cause weakness and paralysis in the lower motor neurons.
Amyotrophic lateral sclerosis (ALS), spinal muscular atrophy , poliomyelitis , and primary lateral sclerosis are all examples of motor neuron diseases
Spinal Muscular Atrophy (SMA) affects about 1 in 10,000 live births, resulting in approximately 1 in 11,000 live births being born with SMA.