Gitelman syndrome combined with growth hormone deficiency: Three cases report

RATIONALE: Gitelman syndrome (GS) is a rare autosomal recessive hereditary salt-losing tubulopathy caused by loss-of-function mutations in the SLC12A3 gene. It is usually characterized by hypokalemia, metabolic alkalosis, hypomagnesemia, and hypocalciuria. There are only a few reports on GS combined...

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Detalles Bibliográficos
Autores principales: Huang, Ke, Dai, Yang-Li, Zhang, Jian-Wei, Zhang, Li, Wu, Wei, Dong, Guan-Ping, Ullah, Rahim, Fei, Yue, Fu, Jun-Fen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
4300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783222/
https://www.ncbi.nlm.nih.gov/pubmed/31577716
http://dx.doi.org/10.1097/MD.0000000000017244

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783222/
https://www.ncbi.nlm.nih.gov/pubmed/31577716
http://dx.doi.org/10.1097/MD.0000000000017244

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