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...

Descripción completa

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

Internet

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

Ejemplares similares