Spina bifida is a type of birth
defect called a neural tube defect. It
occurs when the bones of the spine (vertebrae) don't form properly around part
of the baby's spinal cord. Spina bifida can be mild or severe.
The exact cause of this
birth defect isn't known. Experts think that
genes and the environment are part of the cause. For
example, women who have had one child with spina bifida are more likely to have
another child with the disease. Women who are obese or who have diabetes are
also more likely to have a child with spina bifida.
Your child's symptoms will
depend on how severe the defect is. Most children with the mild form of spina bifida don't have any problems from it.
In many cases, children with meningocele don't have any symptoms.
Children with the most severe form of spina bifida often have spine and brain issues that cause serious problems. They may have:
During pregnancy, you can have a blood test (maternal serum triple or quadruple screen) and an
ultrasound of the developing baby. These tests check for signs of spina bifida and other
problems. If test results suggest a birth
defect, you can choose to have an
amniocentesis. This test helps confirm if the baby has spina bifida.
After birth, a doctor can usually tell if a baby has spina bifida by how the
baby's back looks. If spina bifida is suspected, the doctor may do an
MRI, or a
CT scan to see if the defect is mild or severe.
Most children with the mild form of spina bifida don't need treatment. Children with meningocele may not need treatment either. But children with the most severe form usually need surgery. Sometimes surgery to correct severe spina bifida can be done before a baby is born.
A child who has hydrocephalus will need surgery to put in a drainage tube
called a shunt. It relieves pressure on the brain by draining excess fluid
into the belly. This keeps the swelling from causing more damage to the
Experts such as physical therapists and occupational therapists work with children who have severe spina bifida. The work starts soon after the child's birth. These therapists can teach parents and caregivers how to do exercises and activities with the child.
Some children may need a brace, a
wheelchair, or other aids. Children with bladder control problems may need help using a
catheter each day to prevent infection and kidney damage. As children with severe spina bifida grow, other treatments and surgeries may be needed to manage problems that arise.
There are many ways you
can support your child:
Remember that your needs are important too. Take good care of yourself so you
can stay healthy and have the energy to enjoy your child. Make time for activities you like, even if it's just for a short while each day. And reach out to family, friends, and support groups when you need help.
during pregnancy, a woman can help prevent spina bifida in her child.
Health Tools help you make wise health decisions or take action to improve your health.
Learning about spina bifida:
Testing for spina bifida:
Living with spina bifida:
Easter Seals provides information and services to help
people with disabilities. Its programs include counseling, training, social
clubs, camping, transportation, and referrals. Call for information on the
nearest chapter or to receive a catalog of their publications and
The National Institute of Neurological Disorders and
Stroke (NINDS), a part of the National Institutes of Health, is the leading
U.S. federal government agency supporting research on brain and nervous system
disorders. It provides the public with educational materials and information
about these disorders.
This website is sponsored by the Nemours Foundation. It
has a wide range of information about children's health—from allergies and
diseases to normal growth and development (birth to adolescence). This website
offers separate areas for kids, teens, and parents, each providing
age-appropriate information that the child or parent can understand. You can
sign up to get weekly emails about your area of interest.
The March of Dimes tries to improve the health of babies
by preventing birth defects, premature birth, and early death. March of Dimes
supports research, community services, education, and advocacy to save babies'
lives. The organization's website has information on premature birth, birth
defects, birth defects testing, pregnancy, and prenatal care.
The Spina Bifida Association of America is a voluntary
health agency that provides information about spina bifida to parents and
health professionals to promote public awareness, advocacy, and research. This
organization produces written and audiovisual materials, including a newsletter
and brochures covering topics such as latex allergy and folic acid.
Other Works Consulted
Adzick NS, et al. (2011). A randomized trial of prenatal versus postnatal repair of myelomeningocele. New England Journal of Medicine. Published online February 9, 2011 (doi:10.1056/NEJMoa1014379).
American College of Obstetricians and Gynecologists (2003, reaffirmed 2011). Neural tube defects. ACOG Practice Bulletin No. 44. Obstetrics and Gynecology, 102(1): 203–210.
Ghatan S (2006). Myelomeningocele. In FD Burg et al., eds., Current Pediatric Therapy, 18th ed., pp. 377–380. Philadelphia: Saunders Elsevier.
Liptak GS (2007). Neural tube defects. In ML Batshaw et al., eds., Children with Disabilities, 6th ed., pp. 419–438. Baltimore: Paul H. Brookes Publishing.
Liptak GS, Dosa NP (2010). Myelomeningocele. Pediatrics in Review, 30(31): 443–450.
U.S. Preventive Services Task Force (2009). Folic acid to prevent neural tube defects. Available online: http://www.uspreventiveservicetaskforce.org/uspstf/uspsnrfol.htm.
December 12, 2012
Adam Husney, MD - Family Medicine
& Louis Pellegrino, MD - Developmental Pediatrics
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