Centrotemporal Epilepsy Treatment in Turkey
About Centrotemporal Epilepsy
Key Highlights
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Common and typically benign childhood epilepsy syndrome with an excellent long-term prognosis.Seizures often occur during sleep, minimizing daytime disruption for many children.Highly responsive to anti-seizure medications in most cases.Most children outgrow the condition spontaneously by mid-to-late adolescence.Focuses on preserving normal cognitive development and quality of life.
Who is this surgery for?
- Clinical presentation of focal seizures, often with facial twitching, drooling, and speech arrest, typically during sleep.
- EEG findings showing characteristic centrotemporal (rolandic) spikes.
- Recurrent seizures that interfere with daily activities, safety, or sleep quality.
- Age of onset typically between 3 and 13 years.
- Family history of epilepsy or febrile seizures may support the diagnosis.
How to prepare
- Detailed clinical history taking, including seizure description, frequency, and triggers.
- Neurological examination by the specialist.
- Sleep-deprived or prolonged EEG recording to capture characteristic brain wave patterns.
- In some cases, an MRI brain scan may be performed to rule out other structural causes.
- Discussion with the family and child (if age-appropriate) about diagnosis, treatment options, and expectations.
Risks & possible complications
- Potential side effects from anti-seizure medications, such as drowsiness, dizziness, or behavioral changes.
- Rare breakthrough seizures if medication is not fully effective or doses are missed.
- In very rare cases, atypical evolution or learning difficulties, though the syndrome is typically benign.
- Risk of injury during a seizure, though most occur during sleep in a safe environment.
- Psychological or social impact of having a epilepsy diagnosis.
Recovery & hospital stay
- Recovery from individual seizures is typically rapid, with a quick return to baseline.
- Long-term management involves regular follow-up with the neurologist to monitor medication efficacy and side effects.
- Medication dosage may be adjusted over time based on seizure control and growth of the child.
- Most children can participate fully in school and activities with proper management.
- The goal is eventual medication withdrawal after a prolonged seizure-free period, typically in adolescence.
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Typical hospital stay:
Usually outpatient (0 days)
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Expected recovery time:
Ongoing management; seizures typically resolve in adolescence
Frequently Asked Questions
If you are considering centrotemporal epilepsy in Turkey, these questions and answers can help you make a confident, informed decision.
Popular choices for centrotemporal epilepsy in Turkey include Istinye Üniversitesi Hastanesi Liv, VM Medical Park Pendik Hastanesi, Medical Park Gaziosmanpaşa, Medical Park Bahçelievler, Liv Hospital Ankara, known for experienced specialists and advanced surgical infrastructure.
Look at the doctor’s years of experience, hospital association, patient reviews, and how often they perform centrotemporal epilepsy. MediFyr helps you compare neurologists and book consultations online.
The overall cost depends on hospital category, surgeon’s experience, room type, implant or device used (if any), length of stay, tests, and post-operative care. Our team can help you get cost estimates from multiple hospitals before you decide.
Procedure cost in other countries
Here is an overview of how the estimated cost, hospital stay, and recovery time for centrotemporal epilepsy compare across other countries where we have data.
| Country | Estimated cost range | Typical stay | Recovery time | View details |
|---|---|---|---|---|
| India | USD 55 – USD 275 | Usually outpatient (0 days) | ~ Ongoing management; seizures typically resolve in adolescence | Know More |
| Turkey | USD 410 – USD 2,049 | Usually outpatient (0 days) | ~ Ongoing management; seizures typically resolve in adolescence | Know More |
Top hospitals for Centrotemporal Epilepsy in Turkey
These partner hospitals in Turkey have dedicated neurology teams and experience managing patients undergoing centrotemporal epilepsy.
Istanbul, Turkey
150 Doctors
Anjali Davis is a 9-year-old girl...
Anjali Davis is a 9-year-old girl who loves art and soccer. She lives with her parents and younger brother. For the past six months, Anjali has been experiencing strange episodes, usually just after waking up. She describes a tingling, 'pins and needles' sensation on the right side of her face and tongue, followed by an inability to speak clearly for about a minute, though she remains fully aware. These episodes, happening 2-3 times a week, frightened her and made her anxious about school. Her pediatrician referred her to a pediatric neurologist, Dr. Chen. After reviewing Anjali's detailed description and a normal MRI, Dr. Chen diagnosed her with Benign Rolandic Epilepsy (a type of centrotemporal epilepsy). He recommended starting a low dose of an anti-seizure medication, oxcarbazepine, explaining it was highly effective for her specific condition. Anjali was nervous about taking daily medicine. The treatment experience was positive; the medication was well-tolerated with no side effects. Within two weeks, the episodes stopped completely. At her 3-month follow-up, she remained seizure-free. Her EEG showed significant improvement. Emotionally, Anjali transformed from a fearful, withdrawn child worried about having an episode at school back into her confident, energetic self. Her parents' constant worry lifted, replaced by relief and gratitude for a simple, effective treatment.