Tratamiento anestésico en el síndrome de Kearns-Sayre. Descripción de un caso / Anesthetic management of Kearns-Sayre syndrome. Case report
Rev. esp. anestesiol. reanim
; 68(4): 232-234, Abr. 2021.
Article
in Es
| IBECS
| ID: ibc-232485
Responsible library:
ES1.1
Localization: ES15.1 - BNCS
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.(AU)
ABSTRACT
Kearns-Sayre syndrome is a mitochondrial myopathy characterized 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 anesthesia for a traumatic femoral fracture surgery.(AU)
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Collection:
06-national
/
ES
Database:
IBECS
Main subject:
Physical Examination
/
Kearns-Sayre Syndrome
/
Mitochondrial Diseases
/
Pain Management
/
Inpatients
/
Anesthesiology
Limits:
Humans
/
Male
Language:
Es
Journal:
Rev. esp. anestesiol. reanim
Year:
2021
Document type:
Article