Spinal Muscular Atrophy
What is spinal muscular atrophy (SMA)?
Spinal muscular atrophy is a genetic disease that affects the motor neurons in the
spinal cord, resulting in muscle wasting and weakness.
What causes spinal muscular atrophy?
SMA is an autosomal recessive disease. This means that both males and females are
equally affected, and that two copies of the gene, one inherited from each parent,
are necessary to have the condition.
A gene called survival motor neuron (or SMN) is found to have an abnormal area (either
a deletion or extra copy of the gene) in over 95% of cases of SMA. Symptomatic individuals
of all ages can be tested through DNA studies typically done from a blood sample.
When both parents are carriers, there is a 1 in 4, or 25%, chance, with each pregnancy,
to have a child with SMA. Carrier testing for the general population is technically
difficult and usually available only if a previously affected child in the family
has been studied.
What are the symptoms of spinal muscular atrophy?
Spinal muscular atrophy is sometimes difficult to diagnose, as symptoms can look like
other conditions or medical problems. Each child may experience symptoms differently.
There are 4 types of spinal muscular atrophy based on symptoms and age of onset. The
child may have the following symptoms:
Type I (also called Werdnig-Hoffman or infantile-onset SMA). This is the most severe type of SMA and may be present at birth. Infants have problems
holding their head, sucking, feeding, swallowing, and typically move very little.
The muscles of the chest are also affected. The motion of the tongue is described
as having "worm-like" movements. Death results usually by the age of two to six years
from breathing problems.
Type II (juvenile SMA, intermediate SMA, or chronic SMA). This form of SMA is seen in children from six months to 18 months of age. They typically
have generalized muscle weakness and may require braces, walkers, or a wheelchair
for assistance. Life-expectancy often extends into adulthood.
Type III [also called (Wohlfart-)Kugelberg-Welander or mild SMA]. This form of SMA affects children older than 18 months of age or as late as adolescence.
These children show signs of clumsiness, difficulty walking, mild muscle weakness,
and may have delayed motor development. These children live long into their adult
Type IV. This form of SMA affects adults in their 30s and 40s, resulting in a walking disability.
The symptoms of spinal muscular atrophy may look like other problems or medical conditions.
Always consult your child's doctor for a diagnosis.
How is spinal muscular atrophy diagnosed?
The diagnosis of spinal muscular atrophy is made after the sudden or gradual onset
of specific symptoms and after diagnostic testing. During the physical exam, your
child's doctor will obtain a complete medical history of your child, and he or she
may also ask if there is a family history of any medical problems.
Currently, if the diagnosis of SMA is suspected, genetic testing is usually the first
test done. Diagnostic tests that may be done to confirm the diagnosis of spinal muscular
Blood tests. These include genetic tests and measurements of a muscle enzyme (CK).
Muscle biopsy. A small sample of the muscle is removed and examined to determine and confirm a diagnosis
Genetic tests. Diagnostic tests that evaluate for conditions that have a tendency to run in families.
Electromyogram (EMG). A test that measures the electrical activity of a muscle or a group of muscles. An
EMG can detect abnormal electrical muscle activity due to diseases and neuromuscular
Treatment of spinal muscular atrophy
Your child’s health care provider will figure out the best treatment based on:
How old your child is
His or her overall health and medical history
How sick he or she is
How well your child can handle specific medications, procedures, or therapies
How long the condition is expected to last
Your opinion or preference
There is no cure for spinal muscular atrophy. The key to medically managing spinal
muscular atrophy is through early detection.
The goal of treatment is to prevent respiratory problems and provide adequate nutritional
care to the child since the swallowing and breathing muscles can be affected by this
There are experimental studies that may be available for SMA. Information about these
studies can be found at clinicaltrials.gov.
The extent of the problem is dependent on the severity of the condition and the presence
of other problems that could affect the child. In severe cases, a breathing machine
may be required to help the child breathe easier.
The health care team educates the family after hospitalization on how to best care
for their child at home and outlines specific clinical problems that require immediate
medical attention by his or her doctor. A child with spinal muscular atrophy requires
frequent medical evaluations throughout his or her lifespan.