Immaturité rénale et oligonéphronie du prématuré: conséquences à long terme [Premature kidneys and oligonephronia: long term repercussion]

Détails

ID Serval
serval:BIB_B73F4DDB95D7
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Immaturité rénale et oligonéphronie du prématuré: conséquences à long terme [Premature kidneys and oligonephronia: long term repercussion]
Périodique
Revue medicale suisse
Auteur⸱e⸱s
Wilhelm-Bals A., Chehade H., Girardin E., Gonzalez E., Parvex P.
ISSN
1660-9379 (Print)
ISSN-L
1660-9379
Statut éditorial
Publié
Date de publication
19/02/2014
Peer-reviewed
Oui
Volume
10
Numéro
418
Pages
435-436,438-441
Langue
français
Notes
Publication types: English Abstract ; Journal Article
Publication Status: ppublish
Résumé
The premature has a reduced number of nephrons. This condition, added to an immature renal function at birth, increases the vulnerability to hemodynamic changes, drug toxicity, and nephrocalcinosis. The oligonephronia worsens the risk to present in adulthood, hypertension and renal insufficiency. Nephrocalcinosis appears in the postnatal period, secondary to renal calcifications. This condition increases the risk of further renal endowment. The nephrocalcinosis is closely related to rickets in the premature. Indeed, an excess of vitamin D and calcium, increases the risk of nephrocalcinosis. The early recognition of markers, such as microalbuminuria, hypertension and hypercalciuria, allow targeting prevention measures.
Mots-clé
Adult, Biomarkers/metabolism, Humans, Hypertension/etiology, Hypertension/physiopathology, Infant, Newborn, Infant, Premature, Infant, Premature, Diseases/pathology, Kidney/pathology, Kidney Diseases/etiology, Kidney Diseases/pathology, Nephrocalcinosis/etiology, Nephrocalcinosis/pathology, Nephrons/pathology, Renal Insufficiency/etiology, Renal Insufficiency/physiopathology, Time Factors
Pubmed
Création de la notice
16/04/2021 12:49
Dernière modification de la notice
17/04/2021 6:34
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