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Classic Bartter syndrome complicated with profound growth hormone deficiency: a case report

INTRODUCTION: Classic Bartter syndrome is a salt-wasting tubulopathy caused by mutations in the CLCNKB (chloride channel Kb) gene. Although growth hormone deficiency has been suggested as a cause for persistent growth failure in patients with classic Bartter syndrome, in our opinion the diagnoses of...

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Detalles Bibliográficos
Autores principales:	Adachi, Masanori, Tajima, Toshihiro, Muroya, Koji, Asakura, Yumi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880170/ https://www.ncbi.nlm.nih.gov/pubmed/24377430 http://dx.doi.org/10.1186/1752-1947-7-283

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