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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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| Prif Awduron: | , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
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BioMed Central
2013
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| Mynediad Ar-lein: | 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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