About Spina Bifida
Spina bifida is a neural tube defect (a disorder involving
incomplete development of the brain, spinal cord, and/or their
protective coverings) caused by the failure of the fetus's
spine to close properly during the first month of
pregnancy.
Infants born with Spina Bifida sometimes have an open lesion
on their spine where significant damage to the nerves and
spinal cord has occurred.
Although the spinal opening can be surgically repaired
shortly after birth, the nerve damage is permanent, resulting
in varying degrees of paralysis of the lower limbs.
Even when there is no lesion present there may be improperly
formed or missing vertebrae and accompanying nerve damage. In
addition to physical and mobility difficulties, most
individuals have some form of learning disability.
The three most common types of Spina Bifida are:
myelomeningocele, the severest form, in which the spinal cord
and its protective covering (the meninges) protrude from an
opening in the spine; meningocele in which the spinal cord
develops normally but the meninges protrude from a spinal
opening; and occulta, the mildest form, in which one or more
vertebrae are malformed and covered by a layer of skin.
Spina Bifida may also cause bowel and bladder complications,
and many children with Spina Bifida have hydrocephalus
(excessive accumulation of cerebrospinal fluid in the
brain).
Treatment
There is no cure for Spina Bifida because the nerve tissue
cannot be replaced or repaired. Treatment for the variety of
effects of Spina Bifida may include surgery, medication, and
physiotherapy.
Many individuals with Spina Bifida will need assistive
devices such as braces, crutches, or wheelchairs. Ongoing
therapy, medical care, and/or surgical treatments may be
necessary to prevent and manage complications throughout the
individual's life.
Surgery to close the newborn's spinal opening is generally
performed within 24 hours after birth to minimize the risk of
infection and to preserve existing function in the spinal
cord.
Prognosis
The prognosis for individuals with Spina Bifida depends on
the number and severity of abnormalities. Prognosis is poorest
for those with complete paralysis, hydrocephalus, and other
congenital defects. With proper care, most children with Spina
Bifida live well into adulthood.
Research
Neural tube defects (NTDs) are one of the
most common birth defects. NTDs result when the neural tube
(which includes the spinal cord and brain) fails to close
during the first month of embryonic development.
NTDs include several disorders ranging from spina bifida
(incomplete closure of the bones around the spinal cord that
can lead to paralysis) to a lack of a cranium (the bones of the
head) and its contents, called anencephaly.
Several studies and clinical trials have
shown that 50% or more of NTDs can be prevented if women
consume a folic acid-containing supplement before and during
the early weeks of pregnancy.
Reference for Spina Bifida Article
- MRC
Vitamin Study Research Group. Prevention of neural tube
defects: results of the Medical Research Council Vitamin
Study. Lancet 1991;338:131–7.
- Czeizel AE, Dudás I. Prevention of the
first occurrence of neural-tube defects by periconceptional
vitamin supplementation. N Engl J Med
1992;327:1832–5.
- National Institutes of
Health
Health
Related Websites
The National Cancer
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The National Heart, Lung,
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National Institute on
Aging
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Arthritis and Musculoskeletal and Skin Diseases
National Institute of
Diabetes and Digestive and Kidney Diseases
National Institute on Drug
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National Institute of Mental
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National Institute of
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