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Síndrome de DiGeorge. Tratamiento anestésico.

Authors :
Bellas, Soledad
Marín, Felisa
Sepúlveda, Ana
Source :
Revista Mexicana de Anestesiología. Oct-Dec2011, Vol. 34 Issue 4, p309-312. 4p. 1 Black and White Photograph, 1 Diagram.
Publication Year :
2011

Abstract

Background: 22q11.2 Deletion syndrome is a condition of abnormality development, characterized by a three-megabase microdeletion in chromosome 22q11. This problem is associated with a variety of phenotypes clinicians, including DiGeorge syndrome, which is characterized by cardiovascular, oropharyngeal, immunological, endocrine and neurological disorders. Case report: We report a 12-month age diagnosed as having DiGeorge syndrome who underwent inhalational general anesthesia for the channeling of a central line run by ultrasound. Discussion: We studied the potential problems for the conduct Anesthesia for patients diagnosed with DiGeorge syndrome. [ABSTRACT FROM AUTHOR]

Details

Language :
Spanish
ISSN :
04847903
Volume :
34
Issue :
4
Database :
Academic Search Index
Journal :
Revista Mexicana de Anestesiología
Publication Type :
Academic Journal
Accession number :
73471638