[HTML][HTML] An expert consensus on practical clinical recommendations and guidance for patients with classic Fabry disease
DP Germain, G Altarescu, R Barriales-Villa… - Molecular genetics and …, 2022 - Elsevier
Fabry disease is an X-linked inherited lysosomal disorder that causes accumulation of
glycosphingolipids in body fluids and tissues, leading to progressive organ damage and …
glycosphingolipids in body fluids and tissues, leading to progressive organ damage and …
Anderson–Fabry disease management: role of the cardiologist
M Pieroni, M Namdar, I Olivotto… - European Heart …, 2024 - academic.oup.com
Anderson–Fabry disease (AFD) is a lysosomal storage disorder characterized by glycolipid
accumulation in cardiac cells, associated with a peculiar form of hypertrophic …
accumulation in cardiac cells, associated with a peculiar form of hypertrophic …
Electrocardiographic characteristics and their correlation with echocardiographic alterations in Fabry disease
M Zada, Q Lo, SJ Trivedi, M Harapoz, AC Boyd… - Journal of …, 2022 - mdpi.com
Fabry disease (FD) is an X-linked disorder with α-galactosidase A deficiency. Males (> 30
years) and females (> 40 years) often present with cardiac manifestations, predominantly left …
years) and females (> 40 years) often present with cardiac manifestations, predominantly left …