Familial Bartter's syndrome: report of a case with early manifestations and persistent hypercalciuria

Détails

ID Serval
serval:BIB_31F3228906DF
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Institution
Titre
Familial Bartter's syndrome: report of a case with early manifestations and persistent hypercalciuria
Périodique
Helvetica Paediatrica Acta
Auteur⸱e⸱s
Girardin  E., Favre  L., Vallotton  M. B., Paunier  L.
ISSN
0018-022X
Statut éditorial
Publié
Date de publication
08/1986
Volume
41
Numéro
3
Pages
221-8
Notes
Case Reports
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Aug
Résumé
A case of familial Bartter's syndrome is reported. The child had early and severe clinical and biochemical manifestations. Indomethacin treatment effectively controlled the increased prostaglandin excretion but corrected only partially the potassium and the calcium losses. The child developed during treatment high serum calcium levels which were associated with high parathyroid hormone and calcitriol serum levels.
Mots-clé
Bartter Syndrome/*genetics/pathology/urine Calcitriol/blood Calcium/*urine Child, Preschool Female Humans Hyperaldosteronism/*genetics Indomethacin/therapeutic use Juxtaglomerular Apparatus/pathology Parathyroid Hormone/blood Prostaglandins/urine
Pubmed
Web of science
Création de la notice
15/01/2008 15:27
Dernière modification de la notice
20/08/2019 14:17
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