Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes

Détails

ID Serval
serval:BIB_C3633F32DCA5
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes
Périodique
Journal of Pediatrics
Auteur(s)
Bettinelli  A., Bianchetti  M. G., Girardin  E., Caringella  A., Cecconi  M., Appiani  A. C., Pavanello  L., Gastaldi  R., Isimbaldi  C., Lama  G., Marchesoni  C., Matteucci  C., Patriarca  P., Dinatale  B., Setzu  C., Vitucci  P.
ISSN
0022-3476
Statut éditorial
Publié
Date de publication
01/1992
Peer-reviewed
Oui
Volume
120
Numéro
1
Pages
38-43
Notes
Journal Article --- Old month value: Jan
Résumé
Clinical or biochemical findings were reevaluated in 34 pediatric patients with primary renal tubular hypokalemic metabolic alkalosis. The patients were subdivided into two groups. Bartter syndrome (primary renal tubular hypokalemic metabolic alkalosis with normocalciuria or hypercalciuria) was diagnosed in 18 patients with molar urinary calcium/creatinine ratios greater than 0.20, and Gitelman syndrome (primary renal tubular hypokalemic metabolic alkalosis with magnesium deficiency and hypocalciuria) was diagnosed in 16 patients with molar urinary calcium/creatinine ratios less than or equal to 0.20 and plasma magnesium levels less than 0.75 mmol/L. Some clinically important differences between the groups were observed. Patients with Bartter syndrome were often born after pregnancies complicated by polyhydramnios (8/18) or premature delivery (7/18) and had short stature (11/18) or polyuria, polydipsia, and a tendency to dehydration (16/18) during infancy (12/18) or before school age (18/18). Patients with Gitelman syndrome had tetanic episodes (12/16) or short stature (3/16) at school age (14/16). We conclude that the Bartter and Gitelman syndromes represent two distinct variants of primary renal tubular hypokalemic metabolic alkalosis and are easily distinguished on the basis of urinary calcium levels.
Mots-clé
Alkalosis/blood/*diagnosis/genetics/urine Bartter Syndrome/*diagnosis/genetics Bicarbonates/blood Calcium/blood/*urine Child Child, Preschool Chlorides/blood/urine Creatinine/urine Diagnosis, Differential Female Humans Hypokalemia/blood/*diagnosis/genetics/urine Infant Infant, Newborn Juxtaglomerular Apparatus/pathology Kidney Tubules/pathology Magnesium/urine Magnesium Deficiency/blood/*diagnosis/genetics/urine Male Osmolar Concentration Phosphates/blood Potassium/urine Renin/blood Seizures/physiopathology Sodium/blood/urine Syndrome Tetany/physiopathology
Pubmed
Web of science
Création de la notice
15/01/2008 15:28
Dernière modification de la notice
03/03/2018 21:11
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