This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Infantile spasms

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Infantile spasm (IS), also known as West syndrome, is a unique form of epilepsy present almost entirely during infancy (the first year of life) (1). IS was first described in 1841 by Dr. William James West in a letter to Lancet, describing new infantile convulsions in his 4-month-old son (2).

The condition is characterised by the triad of:

  • clinical flexor or extensor spasms, often involving the extremities and head/neck
  • hypsarrhythmia on electroencephalogram (EEG)
  • subsequent or concurrent intellectual disability (2)

IS is seen in roughly 2-3 per 10,000 live births

  • it is commonly seen between 3 and 8 months of age with a peak incidence at 6 months of age
    • only <10% of cases present in infants older than 1 year of age
    • onset up to 4 years of age has also been reported
  • spasms usually cease by 5 years of age. However other seizure types may occur in as many as 60% even after cessation of IS
  • all ethnic groups are affected, boys are affected slightly more often than girls (ratio of 60:40) (2,3)
  • a family history can be identified in 3%–6% of cases (4)

IS can be classified aetiologically into 3 categories:

  • cryptogenic form
    • underlying cause cannot be identified
    • prior developmental delays
    • normal neurological exam and neuroimaging, and no abnormality in the metabolic evaluation
    • outcomes are more favourable than in symptomatic category
    • early effective treatment will result in improved prognosis
  • symptomatic form
    • underlying structural, metabolic or genetic cause can be identified
    • developmental delay is seen prior to the onset of spasms
  • idiopathic
    • normal development prior to onset of spasms
    • no residual dysfunction
    • normal neuroimaging and normal etiologic evaluation, and normal neurodevelopment.

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.