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 Authors: Ita Pfeferman Heilberg, Cláudia Tótoli, Joaquim Tomaz Calado
Format: Article
Language:English
Published: Instituto Israelita de Ensino e Pesquisa Albert Einstein
Series:Einstein (São Paulo)
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082015000400604&lng=en&tlng=en