A case report of Gitelman syndrome in children

Giltelman syndrome (GS) is an autosomal recessive infectious disease, which is caused by the mutation of SLC12A3 gene encoding thiazide diuretic sensitive sodium chloride cotransporter located in the distal convoluted tubule of the kidney. PATIENT CONCERNS: A 7-year-old and 3-month-old male patient...

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Detalles Bibliográficos
Autores principales: Ying, Jing, Wu, Haixia, Zhang, Ruizhong, Wu, Pengmei, Sui, Fengxuan, Li, Zilong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
6200
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101307/
https://www.ncbi.nlm.nih.gov/pubmed/37058043
http://dx.doi.org/10.1097/MD.0000000000033509

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101307/
https://www.ncbi.nlm.nih.gov/pubmed/37058043
http://dx.doi.org/10.1097/MD.0000000000033509

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