A Rare Cause of Secondary Hypertension; Fabry Disease

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dc.contributor.authorTurkmen, Kultigin
dc.contributor.authorBaloglu, Ismail
dc.contributor.authorSelcuk, Nedim Yilmaz
dc.contributor.authorTonbul, Halil Zeki
dc.date.accessioned2024-02-23T14:41:30Z
dc.date.available2024-02-23T14:41:30Z
dc.date.issued2018
dc.departmentNEÜen_US
dc.description.abstractFabry disease is an x-linked recessive metabolic storage disorder due to the deficiency of lysosomal alpha-galactosidase A, and the subsequent accumulation of glycosphingolipids, throughout the txxiy. Patients usually present with decreased sweating (anhidrosis or hypohidrosis), reddish-purple skin rash in the bathing trunk area (angiokeratomas), personal or family history of burning or hot pain in the hands and feet, particularly during fevers (acroparesthesias), cornea verticillata and proteinuria. In addition, patients can rarely present with severe hypertension. Here, we have reported a Fabry's patient who presented with severe hypertension as an unusual presentation.en_US
dc.identifier.doi10.5262/tndt.2018.2968
dc.identifier.endpage326en_US
dc.identifier.issn1300-7718
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-85053699410en_US
dc.identifier.startpage324en_US
dc.identifier.urihttps://doi.org/10.5262/tndt.2018.2968
dc.identifier.urihttps://hdl.handle.net/20.500.12452/16851
dc.identifier.volume27en_US
dc.identifier.wosWOS:000444468500017en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isotren_US
dc.publisherTurk Nefroloji Diyaliz Transplantasyon Dergisien_US
dc.relation.ispartofTurkish Nephrology Dialysis And Transplantation Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHypertensionen_US
dc.subjectFabry Diseaseen_US
dc.subjectAlpha-Galactosidaseen_US
dc.titleA Rare Cause of Secondary Hypertension; Fabry Diseaseen_US
dc.typeArticleen_US

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