Hypercalciuria and nephrocalcinosis, a feature of Wilson's disease.

Détails

ID Serval
serval:BIB_C84F82821A07
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
Titre
Hypercalciuria and nephrocalcinosis, a feature of Wilson's disease.
Périodique
Nephron
Auteur⸱e⸱s
Hoppe B., Neuhaus T., Superti-Furga A., Forster I., Leumann E.
ISSN
0028-2766 (Print)
ISSN-L
0028-2766
Statut éditorial
Publié
Date de publication
1993
Volume
65
Numéro
3
Pages
460-462
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article
Résumé
Hypercalciuria and nephrocalcinosis are not uncommon in patients with Wilson's disease but have only once been reported as the presenting sign. We diagnosed Wilson's disease in a 17-year-old male patient 6 years after his first episode of gross hematuria and 2 years after detection of hypercalciuria and nephrocalcinosis. Therapy with penicillamine resulted only in a moderate reduction of urinary calcium excretion but oxalate excretion increased.
Mots-clé
Adolescent, Calcium/urine, Hematuria/diagnosis, Hepatolenticular Degeneration/diagnosis, Hepatolenticular Degeneration/drug therapy, Humans, Kidney Calculi/diagnosis, Male, Nephrocalcinosis/diagnosis, Nephrocalcinosis/drug therapy, Oxalates/urine, Oxalic Acid, Penicillamine/therapeutic use, Time Factors
Pubmed
Web of science
Création de la notice
14/03/2011 17:14
Dernière modification de la notice
20/08/2019 16:43
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