DISEASE SCANNER

Global Incurable Diseases Tracker

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Neurological Disease

Epilepsy

MODERATE

Chronic neurological disorder characterized by recurrent, unprovoked seizures due to excessive neuronal activity in brain. Affects 50 million people worldwide. Many types: focal, generalized, unknown onset. Often begins in childhood or after age 65.

Global Affected

50.0M

Countries

111

Symptoms

Seizures (various types)
Temporary confusion
Staring spells
Uncontrollable jerking movements
Loss of consciousness
Psychic symptoms (fear, deja vu)
Tongue biting
Urinary incontinence
Post-ictal confusion
Fatigue

Treatment Options

Anti-seizure medications (ASMs)
Epilepsy surgery
Vagus nerve stimulation (VNS)
Responsive neurostimulation (RNS)
Deep brain stimulation
Ketogenic diet
Modified Atkins diet
Cannabidiol (CBD)
Emergency rescue medications (benzodiazepines)

Risk Factors

1Genetic predisposition
2Brain injury (trauma, stroke)
3Brain infections
4Perinatal insults
5Developmental abnormalities
6Family history
7Febrile seizures (history)
8Central nervous system infections

Diagnostic Methods

  • 1EEG (electroencephalogram)
  • 2Video-EEG monitoring
  • 3Brain MRI
  • 4PET scan
  • 5SPECT
  • 6Neuropsychological testing
  • 7Genetic testing
  • 8Lumbar puncture (rule out infection)

Prognosis

60-70% achieve seizure freedom with ASM. 30-40% drug-resistant epilepsy. Surgery: 50-80% seizure-free in selected patients. Increased mortality (SUDEP: sudden unexpected death in epilepsy). Normal lifespan in most with controlled seizures.

Prevention

  • No primary prevention for genetic epilepsy
  • Head injury prevention
  • Perinatal care optimization
  • Prompt treatment of CNS infections
  • Avoiding seizure triggers (sleep deprivation, alcohol, flashing lights)
  • Medication adherence

Research Status

Newer ASMs (ASM=anti-seizure medications) with better side effect profiles (lacosamide, perampanel, brivaracetam). Epilepsy surgery curative in selected patients. Responsive neurostimulation (RNS). Deep brain stimulation. Ketogenic diet (especially children). Gene therapy for genetic epilepsies. Cannabis-derived medications (Epidiolex for Dravet, Lennox-Gastaut).

Sources

  • https://www.cdc.gov/
  • https://www.ncbi.nlm.nih.gov/books
  • https://www.mayoclinic.org/diseases-conditions
  • https://rarediseases.org/rare-diseases

Medical Disclaimer

This information is for educational purposes only. Always consult healthcare professionals for medical advice, diagnosis, and treatment.