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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

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