8D21

ICD-11 MMS 2026-01

Dyskinetic cerebral palsy

Description

Dyskinetic cerebral palsy, also known as extrapyramidal cerebral palsy is characterised by impairment of voluntary movement because of the presence of interfering involuntary movements, and inappropriate co-contraction of agonist and antagonist muscles (dystonia). This group of disorders includes choreoathetotic cerebral palsy and dystonic cerebral palsy. The former is characterised by large amplitude, involuntary movements of mainly distal limbs (athetosis) with or without small amplitude, fleeting, asymmetric contractions of individual muscle groups (chorea). Dystonic cerebral palsy predominantly affects proximal trunk and limb muscles, which may show slow, persistent movements, leading to the adoption of unusual postures, such as torticollis.

Index terms

  • Dyskinetic cerebral palsy
  • Athetoid cerebral palsy
  • Vogt disease
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  • athetoid cerebral paralysis
  • athetoid cerebrum palsy
  • double athetosis syndrome
  • dyskinetic cerebral paralysis
  • état marbré
  • Congenital athetosis
  • bilateral athetosis
  • double athetosis
  • Bilateral acquired athetosis
  • Dystonic cerebral palsy
  • Status marmoratus

Inclusions

  • Athetoid cerebral palsy

Exclusions from above levels

  • 8B44.0 – Hereditary spastic paraplegia
  • 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

  • 8D20 – Spastic cerebral palsy
  • 8D22 – Ataxic cerebral palsy
  • 8D23 – Worster-Drought syndrome
  • 8D2Y – Other specified cerebral palsy
  • 8D2Z – Cerebral palsy, unspecified

Foundation entity

Dyskinetic cerebral palsy – http://id.who.int/icd/entity/812740125

Part of: 08: Diseases of the nervous system