Spina bifida is a birth defect where the spine and spinal cord don’t form properly, leading to varying degrees of disability depending on severity and location of the defect.
It is a type of neural tube defect that occurs very early in pregnancy when the neural tube fails to close completely.
A congenital condition caused by incomplete closure of the neural tube during early fetal development.
Meaning of the term: Latin for “split spine.”
Types:
Spina bifida occulta: Mildest form, often symptomless, sometimes only a small patch of hair or dimple on the back.
Meningocele: A sac of fluid protrudes through the spine, but the spinal cord is not involved.
Myelomeningocele: Most severe form, where spinal cord and nerves protrude, leading to significant disability.
Causes and Risk Factors
Genetic and environmental factors contribute.
Key risk factors:
Lack of folic acid during pregnancy.
Certain anti-seizure medications.
Obesity or poorly controlled diabetes in the mother.
Symptoms
Visible signs: Hairy patch, dimple, swelling, or dark spot on lower back.
Functional complications:
Difficulty walking or paralysis.
Bladder and bowel control problems.
Hydrocephalus (fluid buildup in the brain).
Tethered spinal cord.
Latex allergy.
Prevention
Folic acid supplementation before and during pregnancy is the most effective preventive measure.
Recommended daily intake: 400 micrograms for women of childbearing age.
Treatment
Surgery: Can be performed after birth or even prenatally to close the spinal opening.
Supportive care: Physical therapy, mobility aids, bladder/bowel management, and treatment for hydrocephalus.
Prognosis: Varies widely; mild cases may live normal lives, while severe cases require lifelong care.