Muscular Atrophy is an inherited genetic condition that affects the
anterior horn cells of the spinal cord. These anterior horn cells are
responsible for controlling voluntary muscles such as crawling, walking,
head and neck control, swallowing and breathing.
are 3 main types of SMA, all of which vary in severity and age of onset.
One common observation is that SMA children are unusually bright and
Diagnosis is usually made before the age of 6 months. This is the most
severe form of SMA. These babies rarely make it to the age of 2, most die
before 1 year due to breathing difficulties like pneumonia. SMA Type 1
babies never are able to lift their heads, or accomplish normal
milestones. Some children have a tongue tremor called tongue
fasciculation. This is seen in virtually no other disease other than SMA.
this disease also affects swallowing and feeding, secretions become
increasingly hard to control and mechanical suctioning is needed. Upon
X-ray of the chest, Type I babies can have a bell shaped rib-cage due to
the general muscle weakness and diaphragmatic breathing (tummy breathing)
is usually made before the age of 2. A less severe disease than Type 1,
these children may be able to sit unsupported. Some are even able to stand
with the help of braces or other aids. Feeding is not usually a problem
with type 2, although some may need to have a feeding tube put in.
type is diagnosed sometime after the age of 18 months, even up to
adolescence. These children are able to stand by themselves and walk, but
may have some difficulties.
SMA is the #1
genetic killer of babies under the age of 2
children with the most severe form often face quickly increasing muscle
weakness, leading to paralysis and death.
One out of 40 people, most unknowingly, carry this deadly gene.
One of every 6,000 children born are affected by SMA.
1 in 4 chance with
each pregnancy of having an affected child (25%)
Some Statistics show SMA to be TWICE as common
discriminate based on age or race or gender
is no cure
specific details on SMA, visit www.smasupport.com!