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Article

Prevalence of Fabry Disease in Familial Mediterranean Fever Patients from Central Anatolia of Turkey.

Biochemical genetics - 1 Aug 2016

Huzmeli Can, Candan Ferhan, Alaygut Demet, Bagci Gokhan, Akkaya Lale, Bagci Binnur, Sozmen Eser Yıldırım, Kurtulgan Hande Kucuk, Kayatas Mansur

Abstract excerpt

Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid metabolism due to deficient or absent lysosomal alpha-galactosidase A (AGALA) activity. FD and familial Mediterranean fever (FMF) have typical clinical similarities, and both diseases may progress to end-stage renal diseases. In this study, we aimed to determine the prevalence of FD in patients with FMF from Central Anatolia of...

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PMID: 27105876
DOI: 10.1007/s10528-016-9731-3

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GLA

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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