Gitelman syndrome combined with complete growth hormone deficiency

Gitelman syndrome is a rare autosomal recessive hereditary salt-losing tubulopathy, that manifests as hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria. It is caused by mutations in the solute carrier family 12(sodium/chloride transporters), member 3 (SLC12A3) gene encoding the thia...

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Detalles Bibliográficos
Autores principales: Min, Se Ra, Cho, Hyun Seok, Hong, Jeana, Cheong, Hae Il, Ahn, Sung Yeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Endocrinology 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4027064/
https://www.ncbi.nlm.nih.gov/pubmed/24904849
http://dx.doi.org/10.6065/apem.2013.18.1.36

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4027064/
https://www.ncbi.nlm.nih.gov/pubmed/24904849
http://dx.doi.org/10.6065/apem.2013.18.1.36

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