Neurology · MU Plovdiv

68. Epilepsy – definition, etiology, pathogenesis. Classification and clinical manifestations of epileptic seizures.

Inside: 7 sections · 3 labelled pictures · 16 flashcards · 10 min

Topic 68 of 75 in the MU Plovdiv syllabus for Neurology (Medicine, Year 4). The free AceMed note covers it in 7 sections, about 1,489 words (10 min of reading), with 16 flashcards.

In this note

  1. Epilepsy. Etiology, Classification, Pathogenesis and Clinical Features
  2. Etiology (8)
  3. Pathogenesis
  4. Epileptic Seizures Classification
  5. Epilepsies Classification (5)
  6. Febrile seizures
  7. Epilepsy - classification, etiology, pathogenesis, clinical features

Epilepsy. Etiology, Classification, Pathogenesis and Clinical Features

Bucal Diazepam should it be diluted? No - Nothing but blood & PH - If you try it'll Perticipate + lose it's activity.

  • Epilepsies are defined as chronic diseases of the brain with various etiologies, which are characterized by repeating epileptic seizures, caused by extreme excitation of damaged neurons.
  • NB A single seizure or a seizure during acute impairment without repetition does NOT mean a diagnosis of epilepsy.

1. G 2. G+E 3. Immune - Glu or NMDA 4. Epilepy Predisposition 5. Acquired 6. Idiopathic 20% (Genetic) 7. Symptom 40% 8. Cryptogenic 40%

Etiology (8)

Multifactorial disease:

  • Genetic: Chromosomal abnormalities, Genetic Metabolic disorders
  • Genetic + environmental factors
  • Immune (antibodies against glutamate receptors)

Acquired: Perinatal damage • Brain Malformations • Tumors • Cranial Trauma • Valvular disease • Inflammation • Alcohol Abuse

  • Acquired (associated with direct or indirect damage – perinatal pathology, brain malformations, tumors, cranial trauma, vascular disease, inflammation, alcohol abuse)
  • Epileptic predisposition
  • Idiopathic (genetic) epilepsy (20%) – with known or suspected genetic defect

Symptomatic: Structural a) Acquired b) Genetic lesion; Functional Metabolic i.e. Leucodystrophies

  • Symptomatic (structural/metabolic) – structural lesions in cases with acquired diseases of CNS (stroke, trauma, infections), structural lesions with genetic causes (some cortical malformations, tuberous sclerosis) and metabolic causes (leucodystrophias, etc.) – in 40%.
  • Cryptogenic (unknown cause) – suspected, but not definitely proven cause in 40%.

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