Angela E. Auletta
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View article: Coexistence of Alport Syndrome and Fabry Disease in a Female with R112H Variant: Early Progression of Fabry Nephropathy
Coexistence of Alport Syndrome and Fabry Disease in a Female with R112H Variant: Early Progression of Fabry Nephropathy Open
Fabry disease (FD) is an X-linked lysosomal disorder caused by GLA mutations, typically associated with glycosphingolipid accumulation and a wide phenotypic spectrum. The p.R112H variant is generally linked to a non-classic predominantly r…
View article: #3648 Renal outcomes of kidney–liver transplantation and liver transplantation in autosomal dominant polycystic kidney disease patients
#3648 Renal outcomes of kidney–liver transplantation and liver transplantation in autosomal dominant polycystic kidney disease patients Open
Background and Aims Autosomal dominant polycystic kidney disease (ADPKD) affects ∼12.5 million people globally and is the fourth leading cause of end-stage kidney disease (ESKD) requiring dialysis or transplantation [1]. It is mainly cause…