Cargando…
Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome
CONTEXT: Gitelman syndrome (GS) is clinically heterogeneous. The genotype and phenotype correlation has not been well established. Though the long-term prognosis is considered to be favorable, hypokalemia is difficult to cure. OBJECTIVE: To analyze the clinical and genetic characteristics and treatm...
Autores principales: | Zhong, F., Ying, H., Jia, W., Zhou, X., Zhang, H., Guan, Q., Xu, J., Fang, L., Zhao, J., Xu, C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531408/ https://www.ncbi.nlm.nih.gov/pubmed/30413979 http://dx.doi.org/10.1007/s40618-018-0966-1 |
Ejemplares similares
-
Hypokalemia, hypomagnesemia, hypocalciuria, and recurrent tetany: Gitelman syndrome in a Chinese pedigree and literature review
por: Xia, Ming‐Feng, et al.
Publicado: (2017) -
A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree
por: Chen, Yixin, et al.
Publicado: (2018) -
Gitelman syndrome
por: Knoers, Nine VAM, et al.
Publicado: (2008) -
Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypes
por: Dong, Bingzi, et al.
Publicado: (2020) -
Clinical and Genetic Characteristics in Patients With Gitelman Syndrome
por: Fujimura, Junya, et al.
Publicado: (2018)