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A Novel Homozygous SCNN1B Variant Causing Severe Systemic Pseudohypoaldosteronism Type 1B in a Saudi Infant: A Case

Ali Alquraishi1, Musa M Saad1, Ruba Alqahtani2

  • 1Department of Pediatrics, Armed Forces Hospital Southern Region (AFHSR), Khamis Mushait, SAU.

Cureus
|May 4, 2026
PubMed

Keywords:
consanguinityepithelial sodium channel (enac)hyperkalemianovel variantsalt-wastingscnn1b genesystemic pseudohypoaldosteronism type 1b

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