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Infantile Pompe Disease Presenting with Severe Hypertrophic Cardiomyopathy: A Case Report

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dc.contributor.authorBayraktar, Suleyman
dc.contributor.authorBAYRAKTAR, Bilge
dc.contributor.authorElevli, Murat
dc.contributor.institutionauthorBAYRAKTAR, BILGE
dc.date.accessioned2020-10-22T15:55:01Z
dc.date.available2020-10-22T15:55:01Z
dc.date.issued2015-09-01T00:00:00Z
dc.description.abstractInfantile Pompe disease (glycogen storage disease type 2) is a fatal disease with autosomal recessive inheritance, leading to hypertrophic cardiomyopathy, hypotonia and respiratory failure. It is a progressive condition due to accumulation of glycogen in the muscles. We aimed to present a case of infantile Pompe disease in a patient who had giant QRS complexes in electrocardiographic monitoring and hypertrophic cardiomyopathy involving the interventricular septum and the left ventricle on echocardiography.
dc.identifier.citationBayraktar S., BAYRAKTAR B., Elevli M., -Infantile Pompe Disease Presenting with Severe Hypertrophic Cardiomyopathy: A Case Report-, HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI, cilt.53, ss.266-268, 2015
dc.identifier.doi10.4274/haseki.2405
dc.identifier.scopus84941557210
dc.identifier.urihttp://hdl.handle.net/20.500.12645/23641
dc.identifier.wosWOS:000216755500021
dc.identifier.wosWOS:000216755500021
dc.subjectInfantile Pompe Disease
dc.titleInfantile Pompe Disease Presenting with Severe Hypertrophic Cardiomyopathy: A Case Report
dc.typeArticle
dspace.entity.typePublication
local.avesis.id4991b613-f451-4db8-a128-8c50ff6025d2
local.indexed.atWOS
local.indexed.atScopus
local.publication.isinternational1
relation.isAuthorOfPublication0c519bac-cbcb-4931-89f6-451ca267749b
relation.isAuthorOfPublication.latestForDiscovery0c519bac-cbcb-4931-89f6-451ca267749b

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