Ratio of Fabry disease in patients with idiopathic left ventricular hypertrophy: A single-center study in Turkey

OBJECTIVE: Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid metabolism which arises due to deficient or absent activity of lysosomal α-galactosidase A (α-Gal A). This may be associated with increased left ventricular (LV) wall thickness and may mimic the morpholo...

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Detalles Bibliográficos
Autores principales: Barman, Hasan Ali, Özcan, Sevgi, Atıcı, Adem, Özgökçe, Caner, Öztürk, Ahmet, Kafalı, Ayşegül Ezgi, Çakar, Nafiye Emel, Tavşanlı, Mustafa Emir, Küçük, Mehmet, Şahin, İrfan, Okuyan, Ertuğrul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2020
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7040871/
https://www.ncbi.nlm.nih.gov/pubmed/32011328
http://dx.doi.org/10.14744/AnatolJCardiol.2019.84782

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7040871/
https://www.ncbi.nlm.nih.gov/pubmed/32011328
http://dx.doi.org/10.14744/AnatolJCardiol.2019.84782

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