Introduction. Renal impairment and neurological symptoms are common manifestations of Fabry disease. Although rare, Fabry disease should be taken into consideration when consulting a patient who presents with neurological and renal impairment, acroparesthesia and fatigue. The aim of this paper is to discuss the case of a female patient presenting with mild systemic symptoms and consequent renal impairment. Case report. The female patient, aged 64, presented for a painful ankle swelling, acroparesthesias, nycturia and fatigue. We diagnosed a gout attack, but found that she had biological signs of renal impairment, aggravated by the use of non-steroidian anti-inflammatory drugs. The search for an etiology of her renal failure proved difficult...
Objectives: Fabry's disease is an X-linked inherited, rare, progressive, lysosomal storage disorder,...
Fabry disease (FD) is a rare, X-linked disorder caused by mutations in the GLA gene encoding the enz...
Fabry disease (FD) is a rare, X-linked disorder caused by mutations in the GLA gene encoding the enz...
Background and objectives: Screening for Fabry disease (FD), an X-linked lysosomal storage disorder,...
Fabry disease is an X-linked genetic deficiency in the alpha-galactosidase enzyme resulting in intra...
Fabry disease (FD) is an X-linked disorder of glycosphingolipid catabolism resulting in the accumula...
Fabry disease (FD) is an X-linked disorder of glycosphingolipid catabolism resulting in the accumula...
BACKGROUND: A 29-year-old white woman with a family history of Fabry disease was referred to a nephr...
Copyright © 2015 H. Trimarchi et al. This is an open access article distributed under the Creative C...
Fabry disease is an X-linked lysosomal storage disorder resulting from the deficiency or absence of ...
Objectives: Fabry's disease is an X-linked inherited, rare, progressive, lysosomal storage disorder,...
Fabry disease (FD) is a rare, X-linked lysosomal storage disorder resulting in decreased or absent a...
Fabry disease (FD) is an X-linked inborn error of glycosphingolipid metabolism due to the deficiency...
BACKGROUND: Fabry disease, an X-linked lysosomal storage disorder caused by deficiency of alpha-gala...
Introduction. Fabry disease is a rare metabolic disorder caused by the genetic deficiency of the lys...
Objectives: Fabry's disease is an X-linked inherited, rare, progressive, lysosomal storage disorder,...
Fabry disease (FD) is a rare, X-linked disorder caused by mutations in the GLA gene encoding the enz...
Fabry disease (FD) is a rare, X-linked disorder caused by mutations in the GLA gene encoding the enz...
Background and objectives: Screening for Fabry disease (FD), an X-linked lysosomal storage disorder,...
Fabry disease is an X-linked genetic deficiency in the alpha-galactosidase enzyme resulting in intra...
Fabry disease (FD) is an X-linked disorder of glycosphingolipid catabolism resulting in the accumula...
Fabry disease (FD) is an X-linked disorder of glycosphingolipid catabolism resulting in the accumula...
BACKGROUND: A 29-year-old white woman with a family history of Fabry disease was referred to a nephr...
Copyright © 2015 H. Trimarchi et al. This is an open access article distributed under the Creative C...
Fabry disease is an X-linked lysosomal storage disorder resulting from the deficiency or absence of ...
Objectives: Fabry's disease is an X-linked inherited, rare, progressive, lysosomal storage disorder,...
Fabry disease (FD) is a rare, X-linked lysosomal storage disorder resulting in decreased or absent a...
Fabry disease (FD) is an X-linked inborn error of glycosphingolipid metabolism due to the deficiency...
BACKGROUND: Fabry disease, an X-linked lysosomal storage disorder caused by deficiency of alpha-gala...
Introduction. Fabry disease is a rare metabolic disorder caused by the genetic deficiency of the lys...
Objectives: Fabry's disease is an X-linked inherited, rare, progressive, lysosomal storage disorder,...
Fabry disease (FD) is a rare, X-linked disorder caused by mutations in the GLA gene encoding the enz...
Fabry disease (FD) is a rare, X-linked disorder caused by mutations in the GLA gene encoding the enz...