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Definition
Spina bifida is a type of birth defect called a neural tube defect. In spina bifida, a baby's spine does not close completely during the first month of pregnancy. In some cases, the spine may poke through the infant's back, usually the lower half. Spina bifida can begin to develop in a fetus even before the mother knows she is pregnant.
There are three kinds of spina bifida:
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Occulta |
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- The least severe form |
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- No symptoms |
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- Small defect in one or more vertebrae |
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- Spinal cord and nerves are normal |
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- Usually no complications |
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Meningocele |
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- A cyst made up of membranes pokes through the open part of the spine |
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- Spinal fluid can leak out |
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- The cyst can be surgically removed |
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- Development after surgery is usually normal |
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Myelomeningocele |
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- This is the most severe form of spina bifida. |
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- A cyst made up of membranes, nerve roots, and sometimes the spinal cord itself pokes through the open spine. |
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- Substantial problems including paralysis and incontinence of bowel and bladder often persist even after surgery. |
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Causes
The cause of spina bifida is unknown. Like most congenital abnormalities, there is a strong hereditary component.
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Risk Factors
A risk factor is something that increases your chance of getting a disease or condition. Most risk factors for spina bifida are related to the mother's health. Risk factors include:
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Low maternal blood level of folic acid at the time of conception |
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Family history of spina bifida |
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A mother who had a previous pregnancy with a neural tube defect |
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Mother's race: Hispanic or Caucasian of European origin |
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Certain medications given during pregnancy |
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Symptoms
The most immediate symptom of meningocele and myelomeningocele is a sac filled with fluid on the baby's spine. The spinal cord and tissues may also protrude through the back.
Infants and children with spina bifida may experience the following long-term symptoms:
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Bowel and bladder problems |
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Frequent urinary tract and other infections |
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Learning disabilities |
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Accumulation of fluid in the brain (hydrocephalus) |
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Scoliosis |
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Latex allergy (from frequent surgeries early in life) |
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Inability to walk |
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Muscle weakness and paralysis of the lower extremities |
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Hip dislocation |
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Foot and ankle deformities. Many children with myelomeningocele are wheelchair bound. |
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Diagnosis
The possibility of spina bifida can be evaluated before birth using a blood test called the maternal serum alpha-fetoprotein (MSAFP) screening test. If this test predicts a high risk of neural tube defects, your doctor will perform two more tests:
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Treatment
Occulta spina bifida requires no treatment.
Meningocele spina bifida is treated with a simple surgery to remove the cyst, after which the child usually develops normally.
Treatment for myelomeningocele spina bifida may include:
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Surgery |
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Extensive surgery is performed on the baby 24-48 hours after birth. During surgery, the nerves, membrane, and spinal cord are put back into the spine and covered with skin. Prompt surgery can prevent further nerve damage but cannot reverse damage that has already occurred. More serious forms of spina bifida may require more surgeries throughout childhood. |
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Physical Therapy |
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Therapists teach parents how to exercise the infant's legs and feet. Walkers, braces, and crutches will often be required for mobility. |
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Ongoing Treatment |
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Complications of spina bifida can be ongoing and extensive. It will be important for you to work with a team of doctors who can provide the best care and support for you and your child. Team members may include: |
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- Neurosurgeons |
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- Orthopedic surgeons |
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- Urologists |
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- Rehabilitation experts |
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- Physical therapists |
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- Psychologists |
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- Social workers |
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Prevention
To help reduce the chance that your baby will be born with spina bifida:
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