Seizures during infancy and childhood Flashcards

1
Q

Types

A
  1. Neonatal epilepsy syndrome
  2. Epilepsy syndromes in children
  3. Benign focal epilepsies
  4. Childhood absence
  5. Juvenile myoclonic
  6. Infantile spasm
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2
Q
  1. Neonatal epilepsy syndrome types
A

Two rare but well-recognized neonatal seizure syndromes are associated with a relatively good prognosis

  1. Benign (self-limited) neonatal seizures
  2. Benign familial neonatal epilepsy

Seizures occur within the first seven days of life
Unifocal clonic

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3
Q
  1. Epilepsy syndromes in children types
A

The Lennox-Gastaut syndrome is associated with severe seizures in childhood
Genetic syndromes and hypoxic ischemic insults.
Children usually present in the first 7 years of life with a syndrome characterized by multiple seizure types, particularly tonic and atonic seizures, an atypical, slow spike and wave pattern on electroencephalogram (EEG), and mental retardation, often with psychotic features

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4
Q

Benign partial/focal epilepsies of childhood

A

Idiopathic syndromes that occur in developmentally and neurologically normal children and have a benign course, remitting prior to adulthood

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5
Q

Absence seizures

petit mal or generalized nonconvulsive seizures

A

The only or most predominant seizure type in several epileptic syndromes, which have markedly different clinical courses and prognoses.

Brief staring episodes with behavioral arrest that may occur tens to hundreds of times daily

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6
Q

Antiepileptic drugs

A

Phenytoin
Phenobarbital
Ethosuximide

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7
Q

Phenytoin

A

good for focal and generalized seizures

SE: gingival hypertrophy

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8
Q

Tx: Lennox Gastaut syndrome

A

Valproic acid, lamotrigine, topiramate

NO carbamazepine

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9
Q

Tx: Benign partial/focal epilepsies of childhood

A

Antiseizure drug treatment is often not recommended, particularly if only focal seizures without impairment of consciousness occur and if the child and family are comfortable with this approach

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