Hypokalemia Associated With a Claudin 10 Mutation: A Case Report
Author:
Funder
NIDDK
Publisher
Elsevier BV
Subject
Nephrology
Reference15 articles.
1. Hypokalemia--consequences, causes, and correction;Weiner;J Am Soc Nephrol,1997
2. Salt-losing tubulopathies in children: what’s new, what’s controversial?;Kleta;J Am Soc Nephrol,2018
3. Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage;Klar;PLoS Genet,2017
4. A novel hypokalemic-alkalotic salt-losing tubulopathy in patients with CLDN10 mutations;Bongers;J Am Soc Nephrol,2017
5. Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome;Hadj-Rabia;Genet Med,2018
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1. Ocular features of NGLY1 deficiency from a prospective longitudinal cohort;Journal of American Association for Pediatric Ophthalmology and Strabismus;2024-06
2. HELIX Syndrome, a Claudinopathy with Relevant Dermatological Manifestations: Report of Two New Cases;Genes;2024-05-26
3. Altered Sweat Composition Due to Changes in Tight Junction Expression of Sweat Glands in Cholinergic Urticaria Patients;International Journal of Molecular Sciences;2024-04-25
4. Claudin-10 Expression and the Gene Expression Pattern of Thick Ascending Limb Cells;International Journal of Molecular Sciences;2024-04-03
5. Clinical and molecular features of four families with CLDN10-related HELIX syndrome;European Journal of Medical Genetics;2023-12
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