Spina Bifida
Spina bifida is one of the most commonly occurring congenital
disorders (birth defects) in the United States, affecting more infants each year
than muscular dystrophy and cystic fibrosis combined. The disorder is caused by
the incomplete development of the fetus’ spine during the first month of
pregnancy.
Spina bifida varies in degree from mild with no symptoms, to
severe with nerve damage and paralysis. Infants born with a more serious degree
of this disorder have open lesions on their spine where significant damage to
nerves and the spinal cord has occurred. The opening can be repaired through
surgery, but the nerve damage is irreversible. Spina bifida can occur anywhere
along the backbone, but is most often found in the small of the back or further
down. There are three types of spina bifida: spina bifida occulta, meningocele,
and myelomeningocele.
Spina bifida occulta
Spina bifida occulta is the mildest and most common form of this disorder.
It usually only involves a minor fault with one or two of the vertebrae and it
usually shows no symptoms AND DOES NOTand does not require treatment. When an
infant is born with spina bifida occulta, the skin is normal and covers the
deformity of the spinal bone. Spina bifida occulta literally means "a hidden
spot on the spine," and for most people, this spot will remain hidden. It has
been estimated that approximately 10 percent of the American population has
spina bifida occulta and that most are not even aware they have it.
Rarely, spina bifida occulta will cause problems when a child
grows to adolescence. By this time in the child’s life, the spinal cord has
become fastened to the backbone, so when the growth spurt of adolescence begins,
the nerves of the spinal cord become stretched. The result can be difficulties
such as weakness and numbness in the legs, bladder infections, and incontinence
(lack of bladder and bowel control). The more the spinal cord is stretched, the
worse the symptoms become. Surgery to relieve these symptoms by reducing the
tension on the spinal cord is simple and often successful.
Meningocele
In this least common type of spina bifida, the meninges (membrane
surrounding the spinal cord) protrude through the opening causing a lump or sac
on the back. More severe than spina bifida occulta, meningocele can nevertheless
be repaired through surgery with little or no nerve damage resulting. The
surgery is performed at any time during infancy. With meningoceles, the spinal
cord has developed normally and is undamaged. The child, therefore, has no
neurological problems.
Myelomeningocele
Myelomeningocele is the most severe form of spina bifida, occurring nearly
once for every 1,000 live births. For infants born with a myelomeningocele, the
spinal cord does not form properly and a portion of the undeveloped cord
protrudes through the back. A sac containing cerebrospinal fluid and blood
vessels surrounds the protruding cord, which is usually not covered by skin so
that the nerves and tissues are exposed. Between 70 and 90 percent of infants
born with myelomeningocele also experience hydrocephalus. Hydrocephalus is an
excess build up of spinal fluid on the brain that will cause brain damage,
seizures, or blindness if it is left untreated. To avoid this, plastic shunts
must be surgically inserted beneath the skin to drain off excess fluid into the
abdominal cavity.
Infants born with myelomeningocele often have paralysis or
weakness below the level of the spinal lesion. This affects the lower limbs
along with problems with bladder and bowel function. In extreme cases, the trunk
and upper extremities are involved.
Prevention, treatment, and management
Because it involves nerve damage, more serious types of spina bifida cannot
be cured. But many experts do believe it can be avoided. Folic acid, a
water-soluble B vitamin often found in leafy green vegetables, plays an
important role in the prevention of spina bifida. Some studies suggest that if
all women of childbearing age took a proper dosage of folic acid (0.4 mg/day),
the incidence of spina bifida could be reduced by up to 75 percent. While spina
bifida does run in families, 95 percent of spina bifida cases have no prior
family history of the disorder.
Children with more severe cases of spina bifida need to learn
mobility skills and need training to learn to manage their bowel and bladder
functions. Some may require catheterization to permit the passage of urine.
These children also require multiple surgeries as they grow up and will need
assistive devices such as braces, crutches and wheelchairs throughout their lives.
Surgery, physiotherapy, and medication are used to treat some of
the effects of spina bifida and may be needed throughout a patient’s life to
prevent and manage certain complications. Children with spina bifida, especially
those who experienced hydrocephalus, sometimes have learning problems. These
learning disorders generally involve difficulty paying attention, expressing or
understanding language, organizing, sequencing, and comprehending math and reading.
Like many other conditions, education about spina bifida and
local support groups can be the greatest tools for managing the disorder and
preventing further complications. The following organizations can provide
additional information about spina bifida:
Spina Bifida Association of America
4590 MacArthur Blvd., NW, Suite 250
Washington D.C. 20007-4226
(800) 621.3141
www.sbaa.org
National Easter Seal Society
230 West Monroe Street, Suite 1800
Chicago, IL 60606
(800) 221.6827
www.easterseals.com/site/PageServer
March of Dimes Birth Defects Foundation
1275 Mamaroneck Avenue
White Plains, NY 10605
(914) 428.7100
www.marchofdimes.com
©Copyright 1995-2009 The Cleveland Clinic Foundation. All rights reserved.
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