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Revista Española de Anestesiología y Reanimación (English Edition) Anesthetic management of Kearns–Sayre syndrome. Case report
Journal Information
Vol. 68. Issue 4.
Pages 232-234 (April 2021)
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30
Vol. 68. Issue 4.
Pages 232-234 (April 2021)
Case report
Anesthetic management of Kearns–Sayre syndrome. Case report
Tratamiento anestésico en el síndrome de Kearns–Sayre. Descripción de un caso
Visits
30
J. Talaván Sernaa,
Corresponding author
jutaser@alumni.uv.es

Corresponding author.
, L. Belmonte Bayoa, E. Gutiérrez Ruedaa, S. Rodríguez Martínezb
a Servicio de Anestesiología y Reanimación, Hospital Obispo Polanco, Teruel, Spain
b Servicio de Urgencias, Hospital Obispo Polanco, Teruel, Spain
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Abstract

Kearns–Sayre syndrome is a mitochondrial myopathy characterised by ophthalmoplegia, pigmentary retinopathy and cardiac conduction abnormalities. This article describes the clinical management of a 50-year-old patient with Kearns–Sayre syndrome who underwent subarachnoid anaesthesia for a traumatic femoral fracture surgery.

Keywords:
Kearns–Sayre syndrome
Mitochondrial disease
Spinal anesthesia
Case management
Resumen

El síndrome de Kearns-Sayre constituye una miopatía mitocondrial que cursa con oftalmoplejia, retinopatía pigmentaria y alteraciones de la conducción cardiaca. Presentamos el caso de un paciente de 50 años de edad con síndrome de Kearns-Sayre intervenido de una fractura de fémur con anestesia subaracnoidea.

Palabras clave:
Kearns-Sayre síndrome
Enfermedad mitocondrial
Anestesia espinal
Tratamiento

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