Safe and Successful Treatment With Agalsidase Beta During Pregnancy in Fabry Disease

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dc.contributor.authorTaşçı, Elif Şenocak
dc.contributor.authorBahçebaşı, Zerrin Bicik
dc.date.accessioned2020-04-30T23:31:45Z
dc.date.available2020-04-30T23:31:45Z
dc.date.issued2015
dc.departmentDÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.descriptionWOS: 000363832600010en_US
dc.descriptionPubMed: 26338166en_US
dc.description.abstractFabry disease, an X-linked lysosomal storage disorder, is caused by alpha-galactosidase A deficiency and leads to accumulation of glycospinhgolipids in most tissues, with life-theratening consequences in the kidney, heart, and cerebrovascular system. Enzyme replacement therapy is available as 2 different preparations: agalsidase alfa and agalsidase beta. Enzyme replacement therapy is started as soon as the diagnosis is confirmed, but there is no data available in the literature about its safety during preganacy. Herein, we described 2 patients with Fabry disease who received agalsidase beta during their pregnancy. This report is important as the data about enzyme replacement therapy during pregnancy is restricted with case reports.en_US
dc.identifier.endpage408en_US
dc.identifier.issn1735-8582
dc.identifier.issn1735-8604
dc.identifier.issue5en_US
dc.identifier.startpage406en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12684/4452
dc.identifier.volume9en_US
dc.identifier.wosWOS:000363832600010en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherIranian Soc Nephrolgyen_US
dc.relation.ispartofIranian Journal Of Kidney Diseasesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectFabry diseaseen_US
dc.subjectpregnancyen_US
dc.subjectagalsidase betaen_US
dc.subjectenzyme replacementen_US
dc.titleSafe and Successful Treatment With Agalsidase Beta During Pregnancy in Fabry Diseaseen_US
dc.typeArticleen_US

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