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A case report on hypoplastic aortic arch.

Author

Kristine Gay S. Tria

Related Institution

Pediatric Cardiology - Philippine Heart Center

Publication Information

Publication Type
Research Project
Date
January 1-December 1, 2016

Abstract

Although anatomically independent, aortic arch hypoplasia is said to be part of coarctation of the aorta.1 It is a rare occurrence in the Philippine Heart Center with only 3 patients diagnosed from 2004 to 2015. This reports a case of a 9-year-old female who presented with a murmur and was diagnosed of congenital heart disease during infancy; however due to financial constraints, surgical management was delayed until childhood. Patch Aortoplasty using a glutaraldehyde-treated pericardium was performed. Aortic arch or tubular hypoplasia presents with a vast array of clinical symptoms from infancy, childhood to adolescence. Definitive management is surgical, which include different techniques and expertise.

Physical Location

LocationLocation CodeAvailable FormatAvailability
Philippine Heart Center Medical Library CR.007.16 Fulltext Print Format

 
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