color spectrum
Skip Navigation Links
For Parents
For Physicians
About Us
Printer Friendly
Bookmark and Share
Myelomeningocele (Spina Bifida)

What is Myelomeningocele (spina bifida) and how does it affect my baby?
Myelomeningocele, the most severe form of spina bifida, is a condition where the fetus’ spinal cord fails to close during development.  This happens between 20 and 28 days of gestation, often before a woman knows she is pregnant.  Because the spinal cord does not close, much of the nerves are exposed, resulting in damage to the cord as the pregnancy continues.

Spina bifida can impact the nervous system, bones and muscles, kidneys and bladder. The location on the spine where the undeveloped area occurs is called the level of the spina bifida. Because nerve damage at this site prevents function below that level, the higher the level, the greater the impact on normal development and function.

The opening in the spinal cord also results in loss of the fluid surrounding the nervous system.  This causes the brain to be positioned further down into the upper spinal column than normal, which is called an Arnold Chiari II malformation.  When this happens, the normal flow of fluid out of the brain is obstructed, causing hydrocephalus, an excess of cerebrospinal fluid within the brain.  After birth, most children with hydrocephalus need to have the extra fluid shunted out of the brain into the abdomen via a ventriculoperitoneal shunt. 

Myelomeningocele affects about 1 in every 1,000 babies, and it ranges in severity.  Some children, with mild cases very low on the spinal cord, can function nearly normally.  More severe cases can cause leg weakness and paralysis, as well as hydrocephalus, and the Arnold Chiari malformation.  People with Myelomeningocele often live long lives, especially if the condition is diagnosed and treated early.

How is Myelomeningocele diagnosed?
At about 15 weeks gestation, a blood test measuring the levels of alpha-fetoprotein can show the physician that there might be a problem.  After that, an ultrasound is performed to detect the Myelomeningocele, but also to detect the conditions that can result from it, such as hydrocephalus, the Chiari malformation, and any problems with the lower extremities.  In all cases, we perform a fetal MRI to gain more detailed information and we perform a fetal echocardiogram to rule out any problem with the heart.

What is the prenatal surgery for Myelomeningocele, and how does it differ from postnatal surgery?
Until recently, the only way to treat Myelomeningocele was surgery after birth.  But, now that the nine-year long Management of Myelomeningocele (MOMS) Trial has been completed, we know that repairing the Myelomeningocele before birth, in the womb, can be beneficial to the baby’s outcome.  The St. Louis Fetal Care Institute has one of the fastest growing fetal myelomeningocele repair programs in the country.

The results of the trial found that prenatal treatment helps reduce, or even eliminate, the major complications of Myelomeningocele—the hydrocephalus, the Chiari malformation, and the lack of movement in the lower extremities.  Diagnosis and repair of the Myelomeningocele before birth can make a big difference in the way the baby develops.

The MOMS trial showed that babies treated in the womb need half the VP shunts, often have reversal of the Arnold-Chiari malformation, and are more likely to walk, at least until 30 months.  Long term follow up data of children treated with prenatal surgery is still being collected, so the benefit beyond 30 months is not fully known.

The operation for open fetal surgery for myelomeningocele repair involves making a small opening in the uterus, then closing the spinal cord opening just like after birth.  The womb is repaired and the mother is in the hospital for four to five days.  The surgery is performed between 19 and 26 weeks of the pregnancy.  Mothers usually stay locally for about two weeks so that we can monitor the pregnancy.  After this, they can return home for delivery.  Because of the weakness caused by the surgery on the uterus, the baby and all future babies have to be delivered by cesarean section.

The benefit to the fetal repair is several fold. 

  1. First, the spine is protected after the fetal repair. 
    • The spine can no longer be damaged during the pregnancy and after. 
  2. Second, the leakage of CSF is stopped. 
    • We think that this causes the brain to rise back into the skull, allowing the fluid within the brain to drain normally and preventing the development of hydrocephlalus.

As with any prenatal surgery, there are risks to both the mother and the baby.  Our team at the St. Louis Fetal Care institute will discuss all of the risks and benefits of the surgery with you and your family, so you can make the best decision for your baby.

The standard care for babies with spina bifida is to repair the defect after birth.  The neurosurgeon closes the opening of the spinal cord, and restores the muscle, skin, and tissue to cover it.  Unfortunately, postnatal surgery cannot restore any of the function that has been lost during the pregnancy, and the damage from hydrocephalus, the Chiari malformation, and/or loss of movement are then permanent.

Click here to learn more about the open fetal myelomenigocele repair, including inclusion and exclusion criteria, and study results.

Click here to learn what to expect if you are having fetal myelomeningocele repair surgery.

How will Myelomeningocele impact my baby after birth?
Myelomeningocele is a disease affecting many parts of the body. There can be a major impact on a baby’s leg and hip movement, depending on the level of the defect.  Problems with hydrocephalus and the Arnold-Chiari malformation need to be followed carefully. 

Because the spinal cord also affects urine and bowel function, these bodily functions often need to be managed to prevent complications. Optimally, babies need to be followed in a spina bifida clinic, where a team of specialists work together to help determine the best course of treatment.

At SSM Cardinal Glennon Children’s Medical Center, a long established spina bifida clinic is available for follow up care after birth.  This is a very specialized clinic in which many doctors of different specialties and nurses are dedicated to the care of these babies. 



Related Survivor Stories...

Lily's Myelomeningocele Story
Lily received open fetal myelomenigocele repair before she was born.

Related News Articles...

Ryleigh is on the move!
The best choice for the Rowes was to wait until after their baby arrived to have MMC surgery.
22nd Fetal Spina Bifida Surgery
Twenty-Second fetal surgery on April 22 may help baby walk after birth
Hysterotomy Thumbnail
Hysterotomy Research Study
St. Louis Fetal Care Institute Launches Hysterotomy Research Study
Update on Stephen
Stephen had fetal spina bifida repair surgery.
Sunshine Bags
A Ray of Sunshine
New Fetal Surgery Study
Pregnant Women With BMI Above 35 Eligible For Fetal Myelomeningocele Repair Study

We are available 24 hours a day to help you!
Call: (314) 268-4037
Toll-Free: (877) SSM FETL
(877) 776-3385
Send Us A Message
Madalyn's Survivor Story
New Fetal Surgery Study
Douglas' Bladder Outlet Obstruction Story
A New Approach To Trisomy