This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Aetiology

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

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:


Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

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.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.