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A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism due to a Novel Homozygous Variant in the SCNN1B Gene.

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Title: A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism due to a Novel Homozygous Variant in the SCNN1B Gene.
Authors: Singin, Berna1 (AUTHOR), Donbaloğlu, Zeynep1 (AUTHOR), Çetiner, Ebru Barsal1 (AUTHOR), Çetin, Kürşat1 (AUTHOR), Zarif, Nurten Özkan2 (AUTHOR), Çelik, Kıymet2 (AUTHOR), Mıhçı, Ercan3 (AUTHOR), Clark, Özden Altıok4 (AUTHOR), Tuhan, Hale1 (AUTHOR), Parlak, Mesut1 (AUTHOR) mesutparlak@akdeniz.edu.tr
Source: Journal of Clinical Research in Pediatric Endocrinology. 2026 Suppl, Vol. 18, p54-58. 5p.
Database: Academic Search Ultimate
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  Data: A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism due to a Novel Homozygous Variant in the SCNN1B Gene.
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+Clinical+Research+in+Pediatric+Endocrinology%22">Journal of Clinical Research in Pediatric Endocrinology</searchLink>. 2026 Suppl, Vol. 18, p54-58. 5p.
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        Value: 10.4274/jcrpe.galenos.2024.2024-10-5
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        Text: English
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      – TitleFull: A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism due to a Novel Homozygous Variant in the SCNN1B Gene.
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            NameFull: Singin, Berna
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              M: 06
              Text: 2026 Suppl
              Type: published
              Y: 2026
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