Spina Bifida

 

What Is It?

Spina bifida is one of a group of disorders called neural-tube defects — malformations of the brain, spinal cord or their coverings. Spina bifida occurs when a fetus’s developing spinal column does not close properly in the first 28 days following fertilization. The disorder can take one of three forms:

  • Spina bifida occulta — The spinal column is not completely closed. This may not cause any symptoms.
  • Meningocele — Part of covering of the spinal cord called the meninges may protrude through an opening in the back.
  • Myelomeningocele — A portion of the spinal cord itself protrudes through an opening in the back.

Meningoceles and myelomeningoceles may appear as saclike structures on an infant’s back at birth. When most people refer to spina bifida, they are referring to the most severe form, myelomeningocele, which occurs in about one in 1,000 births.

Symptoms

The symptoms of spinal bifida can range from mild or severe depending on the severity of the condition itself. In myelomeningocele, the child may have muscle weakness or paralysis below the level of the incompletely closed spinal column, because nerves traveling to the rest of the body from the spinal cord do not function properly. Loss of sensation and an inability to control bladder or bowel function are common. Additionally, cerebrospinal fluid may build up in the brain, leading to a condition called hydrocephalus, which is common in children with myelomeningocele. If left untreated, hydrocephalus can cause brain damage, blindness or seizures.

In addition to physical problems, spina bifida can produce learning problems, including difficulty with the following:

  • Paying attention and expressing or understanding spoken language
  • Reading and mathematical concepts
  • Organizing or sequencing information

Other conditions that may occur more often in those with spina bifida include latex allergy (perhaps related to the multiple surgeries required early in life), tendonitis, obesity, skin problems, depression and gastrointestinal disorders.

Diagnosis

Spina bifida most often is diagnosed at birth when a sac on the baby’s spine is seen. Spina bifida sometimes can be suspected during pregnancy as a result of a test called alpha-fetoprotein, or AFP. Because a number of factors can influence the results of an AFP test, a high level does not establish the diagnosis by itself. If the AFP level is elevated, the test is usually repeated, and if the level is still abnormal, further diagnostic studies such as ultrasound may be done.

Expected Duration

Spina bifida is a lifelong condition. A baby born with spina bifida usually has surgery within the first few days of life to attempt to preserve as much spinal-cord function as possible. Other surgeries and extensive medical care probably will be required throughout the person’s lifetime.

Prevention

Studies have shown that getting enough folic acid dramatically reduces a woman’s chance of giving birth to a baby with spina bifida. According to some estimates, the number of cases of spina bifida would be reduced by 75 percent if all mothers consumed 0.4 milligrams of folic acid each day before becoming pregnant and in the first trimester of pregnancy. Folic-acid supplementation must begin before pregnancy takes place, because the spinal column forms so early after fertilization.

As a result of these studies, in 1992 the U.S. Public Health Service began recommending that all women of childbearing age consume 0.4 milligrams of folic acid daily. Consuming this amount probably requires taking a vitamin supplement, although folic acid is found in dark green leafy vegetables, egg yolks and some fruits and their juices. Since the recommendation was issued, many other foods, including breads and cereals, are now fortified with folic acid.

Treatment

Treatment of spina bifida usually requires surgery to close the opening in the back, to preserve spinal-cord function, and to reduce the risk of infection. Additional surgeries often are required. Shunting, a procedure that drains excess fluid from the brain into the abdomen, controls hydrocephalus and can prevent or reduce many of the consequences of this condition.

Children with spina bifida will need to learn how to use wheelchairs, crutches or braces to improve their mobility. Other interventions can help them become more independent in managing bladder and bowel problems. Educational issues can be addressed with the appropriate professionals.

When To Call A Professional

Doctors will be involved from birth onward in the care of a child with spina bifida. If you notice an abnormal appearance in your child’s back or have concerns about whether his or her neurological function is normal, consult with your child’s pediatrician.

Prognosis

As a result of today’s sophisticated medical techniques and interventions, a child with spina bifida often lives well into adulthood.

Johns Hopkins patient information

Last revised:

Diseases and Conditions Center

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All ArmMed Media material is provided for information only and is neither advice nor a substitute for proper medical care. Consult a qualified healthcare professional who understands your particular history for individual concerns.