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THU598 Pseudohypoaldosteronism Type 2: A New Variant Of A Rare Disease
Disclosure: T.L. Cater: None. L. Borges Espinosa: None. Introduction: Familial hyperkalemia and hypertension syndrome or pseudohypoaldosteronism type 2 (PH2) is a rare monogenic hypertension resulting from WNK1, WNK4, KLHL3, or CUL3 gene mutation. Subsequent interference at the Na-Cl co-symporter, e...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555376/ http://dx.doi.org/10.1210/jendso/bvad114.595 |