8A62.0

ICD-11 MMS 2026-01

Infantile spasms

Description

Syndrome characterised by the subacute onset of brief, repeated seizures with axial or limb flexion, occurring in clusters. EEG shows hypsarrhythmia, i.e., chaotic, high voltage slowing multifocal spikes, with ictal abrupt decremental pattern. Various structural brain pathologies may be present, or no cause may be found. Two-thirds of children have subsequent cognitive deficits.

Coding note from above levels

Use additional code, if desired, to identify the type of seizure.

Index terms

  • Infantile spasms
  • IS -[infantile spasm]
  • West syndrome
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  • salaam spasm
  • salaam tic

Exclusions from above levels

  • MG45 – Syncope
  • 05 – Endocrine, nutritional or metabolic diseases
  • 18 – Complications of pregnancy, childbirth and the puerperium
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  • 19 – Certain conditions originating in the perinatal period
  • 22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

  • 8A62.1 – Lennox-Gastaut syndrome
  • 8A62.2 – Acquired epileptic aphasia
  • 8A62.Y – Other specified epileptic encephalopathies
  • 8A62.Z – Epileptic encephalopathies, unspecified

Foundation entity

Infantile spasms – http://id.who.int/icd/entity/1023597213

Part of: 8A62: Epileptic encephalopathies › 08: Diseases of the nervous system