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Biallelic loss-of-function variants in KCNJ16 presenting with hypokalemic metabolic acidosis
KCNJ16 encodes K(ir)5.1 and acts in combination with K(ir)4.1, encoded by KCNJ10, to form an inwardly rectifying K(+) channel expressed at the basolateral membrane of epithelial cells in the distal nephron. This K(ir)4.1/K(ir)5.1 channel is critical for controlling basolateral membrane potential and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484552/ https://www.ncbi.nlm.nih.gov/pubmed/33840812 http://dx.doi.org/10.1038/s41431-021-00883-0 |
Sumario: | KCNJ16 encodes K(ir)5.1 and acts in combination with K(ir)4.1, encoded by KCNJ10, to form an inwardly rectifying K(+) channel expressed at the basolateral membrane of epithelial cells in the distal nephron. This K(ir)4.1/K(ir)5.1 channel is critical for controlling basolateral membrane potential and K(+) recycling, the latter coupled to Na-K-ATPase activity, which determines renal Na(+) handling. Previous work has shown that Kcnj16(−/−) mice and SS(Kcnj16−/−) rats demonstrate hypokalemic, hyperchloremic metabolic acidosis. Here, we present the first report of a patient identified to have biallelic loss-of-function variants in KCNJ16 by whole exome sequencing who presented with chronic metabolic acidosis with exacerbations triggered by minor infections. |
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