Familial Bartter's syndrome: report of a case with early manifestations and persistent hypercalciuria
Details
Serval ID
serval:BIB_31F3228906DF
Type
Article: article from journal or magazin.
Publication sub-type
Case report (case report): feedback on an observation with a short commentary.
Collection
Publications
Institution
Title
Familial Bartter's syndrome: report of a case with early manifestations and persistent hypercalciuria
Journal
Helvetica Paediatrica Acta
ISSN
0018-022X
Publication state
Published
Issued date
08/1986
Volume
41
Number
3
Pages
221-8
Notes
Case Reports
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Aug
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Aug
Abstract
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.
Keywords
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
Create date
15/01/2008 15:27
Last modification date
20/08/2019 14:17
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