Merhaba!

Kurumsal Kimliğimiz yenilendi.
Yeni web sitemize hoş geldiniz.

Sağlık yolculuğunuz
artık daha kolay.

Sizi daha iyi bilgilendirmek ve
sağlık hizmetlerimize daha hızlı
ulaşmanızı sağlamak için yanınızdayız.


Çakırtepe Hastanesi
Corporate

Spina Bifida

Diagnosis, symptoms, and treatment modalities.

General Information on Spina Bifida

Spina bifida is a congenital neural tube defect occurring during early embryonic development wherein the spinal column and meninges fail to close completely, causing the spinal nerves to be born exposed or protruding within a sac on the infant's back. Maternal folic acid deficiency is a primary etiological factor. In our hospital, multidisciplinary boards comprising Neurosurgery and Pediatric Surgery minimize neurological damage by performing highly specialized surgical closure procedures during the immediate neonatal period.

Disease Details and Frequently Asked Questions

Detailed clinical information regarding the pathology can be accessed under the following headings.
What is Spina Bifida?

Commonly referred to as 'split spine' or 'open spine', it is a birth defect where the neural tube fails to close completely during the first month of pregnancy, leaving a structural gap (opening) in the developing posterior spinal vertebrae.

What is the primary cause (Folic Acid)?

While the exact pathogenesis is multifactorial, the most significant and scientifically proven risk factor is a maternal deficiency of Folic Acid (Vitamin B9) before conception and during the first trimester. Adequate folic acid supplementation prevents this anomaly by approximately 70%.

What are the distinct types?

Spina Bifida Occulta (Hidden): The mildest form; it is a microscopic gap in the bone that is not externally visible and rarely causes neurological deficits.
Meningocele: The protective membranes (meninges) around the spinal cord push out through the opening, forming a fluid-filled sac, but the spinal cord itself remains in place.
Myelomeningocele: The most severe and debilitating form; both the meninges and the spinal cord nerves completely protrude through the defect into a sac on the infant's back.

What kinds of disabilities does it cause?

In its severe forms, the exposed spinal nerves sustain permanent damage in utero, leading to partial or complete paralysis of the lower extremities (inability to walk), profound urinary and fecal incontinence (neurogenic bladder/bowel), and macrocephaly due to the accumulation of cerebrospinal fluid in the brain (Hydrocephalus).

Can it be detected during pregnancy?

Yes. Elevated levels of maternal serum AFP (Alpha-fetoprotein) during the 16th-18th weeks of gestation raise a strong clinical suspicion. A high-resolution Detailed Fetal Ultrasound conclusively visualizes and confirms the spinal defect on the fetus's back.

What are the therapeutic protocols?

For 'open' (myelomeningocele) forms, the infant undergoes emergency neonatal surgery by a Neurosurgeon within the first 24-48 hours of life to prevent fatal CNS infections (meningitis) and further nerve trauma. The neural tissue is carefully repositioned into the spinal canal, and the defect is surgically closed. The ensuing motor and urological deficits demand lifelong multidisciplinary management utilizing physical therapy and intermittent catheterization.

Our health library contents are prepared for informational purposes only and with scientific data available at the time of recording. For all your questions, concerns, diagnosis, or treatment regarding your health, please consult your doctor or a healthcare institution.


You can find all the information regarding your treatment and hospital stay process in this section.

Your Hospital Stay

Your Hospital Stay

Details
Nursing Services

Nursing Services

Details
Patient Admission

Patient Admission

Details
Hospitality Services

Hospitality Services

Details
E-Appointment
E-Consultation
Contact Us