Adult presentation of Bartter syndrome type IV with erythrocytosis

Abstract Bartter syndrome comprises a group of rare autosomal-recessive salt-losing disorders with distinct phenotypes, but one unifying pathophysiology consisting of severe reductions of sodium reabsorption caused by mutations in five genes expressed in the thick ascending limb of Henle, coupled wi...

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Bibliographic Details
Main Author: Heilberg,Ita Pfeferman (author)
Other Authors: Tótoli,Cláudia (author), Calado,Joaquim Tomaz (author)
Format: report
Language:eng
Published: 2015
Subjects:
Bartter syndrome
Hypokalemia
Chloride channels
Case reports
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082015000400604
Country:Brazil
Oai:oai:scielo:S1679-45082015000400604

Internet

http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082015000400604

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