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Aetiology

Authoring team

There are multiple causes for IS which can be divided into the following groups:

  • prenatal
    • accounts for over 40% of cases
    • aetiologies include
      • CNS malformations - focal cortical dysplasia, holoprosencephaly, hemimegalencephaly, Callosal agenesis/Aicardi syndrome
      • chromosomal abnormalities - trisomy 21, Miller-Dieker syndrome
      • single-gene errors
      • neurocutaneous syndrome - tuberous sclerosis complex (TSC), NF1, incontinentia pigmenti
      • congenital central nervous system infections (TORCH)
      • in-born error of metabolism - rarely
  • perinatal
    • aetiologies include
      • hypoxic ischemic encephalopathy
      • hypoglycemia
  • postnatal
    • aetiologies include
      • intracranial infections
      • hypoxic-ischemic insults
      • brain tumours

Note:

  • cortical malformations, hypoxic-ischemic, and tuberous sclerosis are the most common known associated disorders

Reference:


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The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

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