Gordon syndrome and succinylcholine

J Inherit Metab Dis. 2005;28(6):1157-8. doi: 10.1007/s10545-005-0165-z.

Abstract

We present a case of 6-year-old boy who developed severe hyperkalaemia and ventricular tachycardia after administration of succinylcholine. Ventricular tachycardia was defibrillated and Gordon syndrome, which was diagnosed subsequently, was treated successfully. Paediatric patients with underlying metabolic disorders such as Gordon syndrome are at high risk of developing severe hyperkalaemia after succinylcholine administration.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Humans
  • Hyperkalemia / diagnosis*
  • Male
  • Metabolism, Inborn Errors / diagnosis
  • Metabolism, Inborn Errors / metabolism
  • Potassium / metabolism
  • Pseudohypoaldosteronism / diagnosis
  • Risk
  • Succinylcholine / adverse effects*
  • Succinylcholine / therapeutic use
  • Syndrome
  • Tachycardia, Ventricular

Substances

  • Succinylcholine
  • Potassium