A mild and transient form of autosomal recessive pseudohypoaldosteronism type 1 caused by a novel mutation in the SCNN1A gene.
Efthymiadou A, Gautschi I, van Bemmelen MX, Sertedaki A, Giannakopoulos A, Chrousos G, Schild L, Chrysis D. Am J Physiol Endocrinol Metab. 2023 Jul 1; 325(1):E1-E9. Epub 2023 May 3.