Myelomeningocele is a birth defect in which the backbone and spinal canal do not close before birth.
The condition is a type of spina bifida.
Normally, during the first month of a pregnancy, the two sides of the baby's spine (or backbone) join together to cover the spinal cord, spinal nerves, and meninges (the tissues covering the spinal cord). The developing brain and spine at this point are called the neural tube. Spina bifida refers to any birth defect in which the neural tube in the area of the spine fails to close completely.
Myelomeningocele is a neural tube defect in which the bones of the spine do not completely form. This results in an incomplete spinal canal. The spinal cord and meninges (the tissues covering the spinal cord) protrude from the child's back.
Myelomeningocele may affect as many as 1 out of every 4,000 infants.
The rest of spina bifida cases are most commonly:
Other congenital disorders or birth defects may also be present in a child with myelomeningocele. Eight out of ten children with myelomeningocele have hydrocephalus.
Other disorders of the spinal cord or musculoskeletal system may be seen, including:
The cause of myelomeningocele is not known. However, low levels of folic acid in a woman's body before and during early pregnancy appear to play a part in this type of birth defect. Folic acid (or folate) is important for development of brain and spinal cord.
If a child is born with myelomeningocele, future children in that family have a higher risk than the general population. However, in many cases, there is no family connection. Factors such as diabetes, obesity, and the use of anti-seizure medicines in the mother may increase the risk of this defect.
A newborn with this disorder will have an open area or a fluid-filled sac on the mid to lower back.
Symptoms may include:
Other signs and/or symptoms may include:
Prenatal screening can help detect this condition. During the second trimester, pregnant women can have a blood test called the quadruple screen. This test screens for myelomeningocele, Down syndrome, and other congenital diseases in the baby. Most women carrying a baby with spina bifida will have an increased level of a protein called maternal alpha fetoprotein (AFP).
If the quadruple screen test is positive, further testing is needed to confirm the diagnosis.
Such tests may include:
Myelomeningocele can be seen after the child is born. A neurologic exam may show that the child has loss of nerve-related functions below the defect. For example, watching how the infant responds to pinpricks at various locations may tell where the baby can feel the sensations.
Tests done on the baby after birth may include x-rays, ultrasound, CT, or MRI of the spinal area.
The health care provider may suggest genetic counseling. In some cases where a severe defect is detected early in the pregnancy, termination (abortion) may be considered. However, intrauterine surgery to close the defect (before the baby is born) may reduce the risk of some later complications.
After your baby is born, surgery to repair the defect is most often suggested within the first few days of life. Before surgery, the infant must be handled carefully to reduce damage to the exposed spinal cord. This may include:
Children who also have hydrocephalus may need a ventriculoperitoneal shunt placed. This will help drain the extra fluid from the ventricles (in the brain) to the peritoneal cavity (in the abdomen).
Antibiotics may be used to treat or prevent infections such as meningitis or urinary tract infections.
Most children will need lifelong treatment for problems that result from damage to the spinal cord and spinal nerves.
Follow-up exams generally continue throughout the child's life. These are done to:
Visiting nurses, social services, support groups, and local agencies can provide emotional support and assist with the care of a child with a myelomeningocele who has significant problems or limitations.
Taking part in a spina bifida support group may be helpful.
A myelomeningocele can most often be surgically corrected, but the affected nerves may still not function normally. The higher the location of the defect on the baby's back, the more nerves will be affected.
With early treatment, length of life is not severely affected. Kidney problems due to poor drainage of urine are the most common cause of death.
Most children with myelomeningocele will have normal intelligence. However, because of the risk of hydrocephalus and meningitis, more of these children will have learning problems and seizure disorders.
New problems within the spinal cord can develop later in life, especially after the child begins growing rapidly during puberty. This can lead to more loss of function as well as orthopedic problems such as scoliosis, foot or ankle deformities, dislocated hips, and joint tightness or contractures.
Many people with myelomeningocele primarily use a wheelchair.
Complications of spina bifida may include:
This list may not be all-inclusive.
Call your provider if:
Folic acid supplements may help reduce the risk of neural tube defects such as myelomeningocele. It is recommended that any woman considering becoming pregnant take 0.4 mg of folic acid a day. Pregnant women with high risk need higher dosage.
It is important to remember that folic acid deficiencies must be corrected before becoming pregnant, because the defects develop very early.
Women who plan to become pregnant may be screened to determine the amount of folic acid in their blood.
Reviewed By: Kimberly G. Lee, MD, MSc, IBCLC, Associate Professor of Pediatrics, Division of Neonatology, Medical University of South Carolina, Charleston, SC. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.