Learn about Rasmussen Syndrome Treatment in Turkey — how it works, who it is for, recovery timelines, and what to expect before and after surgery. Compare hospitals and doctors experienced in Rasmussen Syndrome and request assistance for cost estimates or appointments.

About Rasmussen Syndrome

Rasmussen syndrome is a rare, chronic neurological disorder primarily affecting children, characterized by progressive inflammation of one hemisphere of the brain. It is not a single procedure but a diagnosis and management pathway led by a neurologist. The condition causes frequent and severe seizures (epilepsia partialis continua), cognitive decline, and progressive weakness on one side of the body. Diagnosis involves a combination of clinical evaluation, electroencephalogram (EEG), and magnetic resonance imaging (MRI) to identify characteristic unilateral brain atrophy. Treatment is complex and multidisciplinary, focusing on controlling seizures with anti-epileptic drugs, immunotherapy to reduce inflammation, and in severe, drug-resistant cases, surgical intervention such as functional hemispherectomy to disconnect the affected hemisphere.

Key Highlights

    Provides a definitive diagnosis for a complex and rare neurological condition.Enables a structured, multi-modal treatment plan to manage seizures and inflammation.Can lead to significant seizure reduction, especially when surgical options like hemispherectomy are considered for drug-resistant cases.Involves a specialized team approach led by a neurologist for comprehensive care.

Who is this surgery for?

  • Frequent, focal motor seizures (epilepsia partialis continua) that are difficult to control with medication.
  • Progressive neurological deficits, such as weakness (hemiparesis) or cognitive decline, localized to one side of the body.
  • MRI findings showing progressive atrophy or inflammation confined to one cerebral hemisphere.
  • EEG results indicating persistent, unilateral brain hemisphere dysfunction.
  • Onset typically in childhood, though adult-onset cases are rarely reported.

How to prepare

  • Comprehensive neurological examination and detailed history of seizure frequency and type.
  • Long-term video-EEG monitoring to capture and localize seizure activity.
  • High-resolution MRI of the brain to assess for unilateral atrophy or inflammation.
  • Neuropsychological testing to evaluate cognitive function and baseline abilities.
  • Discussion with a multidisciplinary team, including epileptologists and neurosurgeons, to plan the treatment pathway.

Risks & possible complications

  • Progression of the disease leading to permanent neurological deficits like hemiplegia, vision loss, or speech impairment.
  • Cognitive and developmental regression despite treatment.
  • Side effects from long-term use of anti-epileptic drugs or immunosuppressive therapies.
  • Risks associated with surgical interventions (if required), including infection, bleeding, or further neurological impairment.
  • Psychological and social impact on the patient and family due to the chronic nature of the condition.

Recovery & hospital stay

  • Recovery is a long-term process focused on managing the chronic condition, not a post-procedure event.
  • Involves careful titration of medications to control seizures while minimizing side effects.
  • Regular follow-up with the neurologist for clinical assessments and repeat EEG/MRI scans.
  • Intensive physical, occupational, and speech therapy to maximize function and adapt to any neurological deficits.
  • For patients undergoing hemispherectomy surgery, recovery involves a specialized inpatient rehabilitation program lasting several weeks to months.
  • checked Typical hospital stay: Varies widely (0 for diagnosis; 2-4 weeks for surgical management)
  • checked Expected recovery time: Ongoing chronic management; surgical recovery 3-6 months

Frequently Asked Questions

If you are considering rasmussen syndrome in Turkey, these questions and answers can help you make a confident, informed decision.

Procedure cost in other countries

Here is an overview of how the estimated cost, hospital stay, and recovery time for rasmussen syndrome compare across other countries where we have data.

Country Estimated cost range Typical stay Recovery time View details
India USD 1,652 – USD 8,809 Varies widely (0 for diagnosis; 2-4 weeks for surgical management) ~ Ongoing chronic management; surgical recovery 3-6 months Know More
Turkey USD 12,293 – USD 65,565 Varies widely (0 for diagnosis; 2-4 weeks for surgical management) ~ Ongoing chronic management; surgical recovery 3-6 months Know More

Top hospitals for Rasmussen Syndrome in Turkey

These partner hospitals in Turkey have dedicated neurology teams and experience managing patients undergoing rasmussen syndrome.

  • Star
  • Star
  • Star
  • Star
  • Star
51+ Rating

Istinye Üniversitesi Hastanesi Liv

  • IconIstanbul, Turkey
  • Icon140 Doctors
  • Star
  • Star
  • Star
  • Star
  • Star
12+ Rating

Liv Hospital Ankara

  • IconIstanbul, Turkey
  • Icon140 Doctors
  • Star
  • Star
  • Star
  • Star
  • Star
112+ Rating

Liv Hospital Bahçeşehir

  • IconIstanbul, Turkey
  • Icon38 Doctors
PATIENT REVIEW

Krishna Saxena, a 12-year-old boy from...

Krishna Saxena, a 12-year-old boy from a close-knit family in Mumbai, was a bright and active student who loved cricket. His parents first noticed subtle changes when he was 9, occasional clumsiness, dropping his bat, and a brief, uncharacteristic stare. Over three years, these episodes evolved into severe, debilitating seizures affecting the left side of his body, paralyzing his arm and leg for hours afterward. Despite trying seven different anti-epileptic drugs, the seizures worsened, and MRI scans revealed progressive atrophy of the right hemisphere of his brain. His neurologist, Dr. Iyer, explained that Krishna had Rasmussen's encephalitis, a rare, inflammatory disease attacking one brain hemisphere. The only curative option was a functional hemispherectomy, a disconnection surgery to isolate the diseased right hemisphere and stop the seizures. The family was terrified at the prospect of such a major brain surgery. The 10-hour procedure was successful. After a challenging month in the hospital, Krishna began intensive rehabilitation. He regained the ability to walk with a slight limp, and his speech and cognition, managed by his healthy left hemisphere, remained sharp. While his left hand has limited function, he has been seizure-free for 18 months. The emotional journey was harrowing, his parents grappled with guilt and fear of losing their son's spark. Post-surgery, seeing Krishna smile, return to school with accommodations, and cheer for his cricket team again has filled them with profound relief and hope for his future.