Spina Bifida and Anencephaly (cont.)
In this Article
- Introduction to spina bifida
- What is spina bifida?
- What are the different types of spina bifida?
- What causes spina bifida?
- What are the signs and symptoms of spina bifida?
- What are the complications of spina bifida?
- How is spina bifida diagnosed?
- How is spina bifida treated?
- Can spina bifida be prevented?
- What is the prognosis for spina bifida?
- What research is being done on spina bifida?
- Where can I get more information?
How is spina bifida diagnosed?
In most cases, spina bifida is diagnosed prenatally, or before birth. However, some mild cases may go unnoticed until after birth (postnatal). Very mild forms (such as spina bifida occulta), in which there are no symptoms, may never be detected.
The most common screening methods used to look for spina bifida during pregnancy are second trimester (16th to 18th weeks of gestation) maternal serum alpha fetoprotein (MSAFP) screening and fetal ultrasound. The MSAFP screen measures the level of a protein called alpha-fetoprotein (AFP), which is made naturally by the fetus and placenta. During pregnancy, a small amount of AFP normally crosses the placenta and enters the mother's bloodstream. If abnormally high levels of this protein appear in the mother's bloodstream it may indicate that the fetus has an "open" (not skin-covered) neural tube defect.
The MSAFP test, however, is not specific for spina bifida and requires correct gestational dates to be most accurate; it cannot definitively determine that there is a problem with the fetus. If a high level of AFP is detected, the doctor may request additional testing, such as an ultrasound or amniocentesis to help determine the cause. Amniocentesis is a medical procedure in which the doctor removes and tests samples of fluid from the amniotic sac that surrounds the fetus. Although amniocentesis cannot reveal the severity of spina bifida, finding high levels of AFP may indicate that the disorder is present.
The second trimester MSAFP screen described above may be performed alone or as part of a larger, multiple-marker screen. Multiple-marker screens look not only for neural tube defects, but also for other birth defects, including Down syndrome and other chromosomal abnormalities. First trimester screens for chromosomal abnormalities also exist but signs of spina bifida are not evident until the second trimester when the MSAFP screening is performed.
Mild cases of spina bifida (ooulta; closed) not diagnosed during prenatal testing may be detected postnatally by X-ray during a routine examination. Doctors may use magnetic resonance imaging (MRI) or a computed tomography (CT) scan to get a clearer view of the spine and vertebrae. Individuals with the more severe forms of spina bifida often have muscle weakness in their feet, hips, and legs. If hydrocephalus is suspected, the doctor may request a CT scan and/or X-ray of the skull to look for extra cerebrospinal fluid inside the brain.
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