Renal disease in Fabry patients.

Détails

ID Serval
serval:BIB_AC156C5DB5BA
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Titre
Renal disease in Fabry patients.
Périodique
Journal of Inherited Metabolic Disease
Auteur⸱e⸱s
Grünfeld J.P., Lidove O., Joly D., Barbey F.
ISSN
0141-8955 (Print)
ISSN-L
0141-8955
Statut éditorial
Publié
Date de publication
2001
Peer-reviewed
Oui
Volume
24
Numéro
Suppl. 2
Pages
71-74
Langue
anglais
Notes
Publication types: Journal Article ; ReviewPublication Status: ppublish
Résumé
Renal dysfunction is a major complication in hemizygous males with Fabry disease. This often results in end-stage renal failure (ESRF), requiring dialysis or transplantation, on average 10 years after the start of renal impairment. ESRF usually occurs between 40 and 50 years of age, but may occur much earlier. Although progression of renal disease can be rapid, it is variable and may depend on whether there is residual alpha-galactosidase enzyme activity and on environmental or genetic factors. Significant renal disease is much less common in women carriers of the disease. However, renal changes do occur, which may progress to ESRF as in male patients.
Mots-clé
Fabry Disease/complications, Fabry Disease/genetics, Female, Heterozygote, Homozygote, Humans, Kidney Diseases/etiology, Kidney Diseases/genetics, Male
Pubmed
Web of science
Création de la notice
09/02/2012 15:43
Dernière modification de la notice
20/08/2019 16:16
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