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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...
Autores principales: | Adachi, Masanori, Tajima, Toshihiro, Muroya, Koji, Asakura, Yumi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
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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