Sydenham's chorea: a practical overview of the current literature

Pediatr Neurol. 2010 Jul;43(1):1-6. doi: 10.1016/j.pediatrneurol.2009.11.015.

Abstract

Sydenham's chorea is characterized by uncoordinated movements, emotional instability, and hypotonia. It can occur up to several months after group A beta-hemolytic Streptococcus infection. A diagnosis of Sydenham's chorea in a patient with acute chorea involves an application of the Jones criteria and the exclusion of other causes of chorea. In patients with an atypical history or hemichorea, cranial magnetic resonance imaging is indicated to exclude other cerebral pathologies. A pathogenesis has not been elucidated, and therapy has not been investigated in placebo-controlled trials. Antibiotic treatment and a 2-week or 3-week schedule of antibiotic prophylaxis are recommended. If the chorea is severe, valproate or carbamazepine can be effective. In more severely affected patients, dopamine receptor blocking agents or corticosteroids can be used.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Anticonvulsants / therapeutic use
  • Carbamazepine / therapeutic use
  • Child
  • Chorea / diagnosis*
  • Chorea / etiology
  • Chorea / therapy
  • Humans
  • Valproic Acid / therapeutic use

Substances

  • Anticonvulsants
  • Carbamazepine
  • Valproic Acid