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The Prevalence of Fabry Disease Among Turkish Patients with Non-Obstructive Hypertrophic Cardiomyopathy: Insights from a Screening Study

dc.contributor.authorAvci, Burcak Kilickiran
dc.contributor.authorIkitimur, Baris
dc.contributor.authorKarpuz, Hakan
dc.contributor.authorDurmaz, Eser
dc.contributor.authorAtici, Adem
dc.contributor.authorBarman, Hasan Ali
dc.contributor.authorAslan, Serkan
dc.contributor.authorCeylaner, Serdar
dc.date.accessioned2021-03-03T20:22:36Z
dc.date.available2021-03-03T20:22:36Z
dc.date.issued2019
dc.identifier.citationBarman H. A. , Ikitimur B., Avci B. K. , Durmaz E., Atici A., Aslan S., Ceylaner S., Karpuz H., "The Prevalence of Fabry Disease Among Turkish Patients with Non-Obstructive Hypertrophic Cardiomyopathy: Insights from a Screening Study", BALKAN MEDICAL JOURNAL, cilt.36, sa.6, ss.354-358, 2019
dc.identifier.issn2146-3123
dc.identifier.otherav_5998e5a2-bd1e-4b36-b4e3-c78a638d1aa5
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/63029
dc.identifier.urihttps://doi.org/10.4274/balkanmedj.galenos.2019.2019.5.125
dc.description.abstractAims: Fabry disease is an X-linked lysosomal storage disorder due to a deficiency of the alpha-galactosidase A enzyme. Cardiac involvement is present in over 60% of adult cases of Fabry disease. Hypertrophic cardiomyopathy without left ventricular outflow tract obstruction is the most common phenotype. The aim of the study was to screen adult patients with hypertrophic cardiomyopathy without left ventricular outflow tract.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectTIP, GENEL & İÇECEK
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectTemel Tıp Bilimleri
dc.titleThe Prevalence of Fabry Disease Among Turkish Patients with Non-Obstructive Hypertrophic Cardiomyopathy: Insights from a Screening Study
dc.typeMakale
dc.relation.journalBALKAN MEDICAL JOURNAL
dc.contributor.departmentIstanbul Okineydani Training & Res Hosp , ,
dc.identifier.volume36
dc.identifier.issue6
dc.identifier.startpage354
dc.identifier.endpage358
dc.contributor.firstauthorID270375


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