Cargando…
Mutations in CLDN2 Are Not a Common Cause of Pediatric Idiopathic Hypercalciuria in Canada
BACKGROUND: Hypercalciuria is the most common risk factor for kidney stone formation, including in pediatric patients. However, the etiology is often unknown and children are frequently diagnosed with idiopathic hypercalciuria. Nearly 50% of children with hypercalciuria have a first-degree relative...
Autores principales: | Ulrich, Emma H., Harvey, Elizabeth, Morgan, Catherine J., Pinsk, Maury, Erickson, Robin, Robinson, Lisa A., Alexander, R. Todd |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125053/ https://www.ncbi.nlm.nih.gov/pubmed/35615069 http://dx.doi.org/10.1177/20543581221098782 |
Ejemplares similares
-
Two novel mutations of the CLDN16 gene cause familial hypomagnesaemia with hypercalciuria and nephrocalcinosis
por: Hanssen, Oriane, et al.
Publicado: (2014) -
Should pediatric idiopathic hypercalciuria be treated with hypocalciuric agents?
por: Penido, Maria Goretti Moreira Guimarães, et al.
Publicado: (2021) -
A novel CLDN16 mutation in a large family with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis
por: Deeb, Asma, et al.
Publicado: (2013) -
Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
por: García‐Castaño, Alejandro, et al.
Publicado: (2020) -
Systematic analysis of global health research funding in Canada, 2000–2016
por: Hoffman, Steven J., et al.
Publicado: (2019)