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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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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3880170/ https://ncbi.nlm.nih.gov/pubmed/24377430 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-7-283 |
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