Abstract
Fabry disease starts as fever of unknown origin (FUO) in almost 20% of
cases. Inflammation parameters are usually variable. Abnormalities in thermal
autoregulation can be true when fever is associated with acroparesthesia and paroxysmal
abdominal pain. Otherwise, in the presence of signs and
symptoms of chronic inflammation, cytokine secretion and activation is probably due to
endothelial and macrophage Gb3 lysosomal storage; proteinuria (less than 1
g/24 hours) and vascular damage are often present, especially in those patients developing
chronic kidney disease and/or cerebrovascular ischemic disease. Diagnosis of Fabry
disease can be simplified by investigating patient's clinical history regarding the
presence of angiokeratomas, cornea verticillata, deafness and/or cardiomyopathy.
Lingua originale | English |
---|---|
pagine (da-a) | 12-15 |
Numero di pagine | 4 |
Rivista | GIORNALE DI TECNICHE NEFROLOGICHE & DIALITICHE |
Volume | 2017 |
Stato di pubblicazione | Pubblicato - 2017 |
Keywords
- Fabry disease