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Select item 115666861.

Pseudohypoaldosteronism type II and sensory neuropathy associated with a heterozygous pathogenic variant in KLHL3 gene, a case report

J.B. Davion, I. Coku, A. Wissocq, A. Genet, J. Poupart, L. Defebvre, V. Huin

Heliyon. 2024 Nov 15; 10(21): e39891. Published online 2024 Oct 29. doi: 10.1016/j.heliyon.2024.e39891

PMCID:: PMC11566686

Article PDF–294K

Select item 114131082.

Transient secondary pseudo-hypoaldosteronism in infants with urinary tract infections: systematic literature review

Céline Betti, Camilla Lavagno, Mario G. Bianchetti, Lisa Kottanattu, Sebastiano A. G. Lava, Federica Schera, Marirosa Cristallo Lacalamita, Gregorio P. Milani

Eur J Pediatr. 2024; 183(10): 4205–4214. Published online 2024 Jul 10. doi: 10.1007/s00431-024-05676-3

PMCID:: PMC11413108

Article PDF–1.1M

Select item 114089733.

Pseudohypoaldosteronism Type 1b in a Saudi Female Infant Due to Homozygous Variant Gene Mutation in SCNN1A: A Case Report

Ali Alquraishi, Abdullah Alshahrany, Badriah G Alasmari, Ashwaq Hommadi, Mohammed Alomari

Cureus. 2024 Aug; 16(8): e67165. Published online 2024 Aug 19. doi: 10.7759/cureus.67165

PMCID:: PMC11408973

Article PDF–110K

Select item 112561224.

Pseudohypoaldosteronism and acquired renal aldosterone resistance with hyperkalemic type IV renal tubular acidosis in 2 cats

Christina L. Marino, Jonathan D. Foster

J Vet Intern Med. 2024 Jul-Aug; 38(4): 2344–2347. Published online 2024 May 2. doi: 10.1111/jvim.17098

PMCID:: PMC11256122

Article PDF–329K

Select item 111361035.

D. Landau

Cell Mol Life Sci. 2006 Sep; 63(17): 1962–1968. Published online 2006 Jun 30. doi: 10.1007/s00018-006-6011-0

PMCID:: PMC11136103

Article PDF–153K

Select item 110600186.

Autosomal Dominant Pseudohypoaldosteronism Type 1 in a Newborn With Failure to Thrive

Sunil Krishna, Mary Augustian

Cureus. 2024 Apr; 16(4): e59356. Published online 2024 Apr 30. doi: 10.7759/cureus.59356

PMCID:: PMC11060018

Article PDF–118K

Select item 110562787.

Pseudohypoaldosteronism Type 1B and Cohen Syndrome: Novel Mutation, Unusual Combination, and Presentation

Yassin Alsaleh, Hussain A Al Ghadeer, Aida Aljabri, Zahra Alhashim, Moneera Mohamed, Fadi Busaleh, Fatimah A Alramadhan, Manal M Alghazal

Cureus. 2024 Mar; 16(3): e57217. Published online 2024 Mar 29. doi: 10.7759/cureus.57217

PMCID:: PMC11056278

Article PDF–236K

Select item 109821188.

A case of secondary pseudohypoaldosteronism that presented as poor weight gain

Keisuke Goshima, Hiroshi Tamura, Yuko Hidaka, Keishiro Furuie, Shohei Kuraoka

Clin Case Rep. 2024 Apr; 12(4): e8722. Published online 2024 Mar 31. doi: 10.1002/ccr3.8722

PMCID:: PMC10982118

Article PDF–1.6M

Select item 108748879.

Pseudohypoaldosteronism Type II or Gordon Syndrome: A Rare Syndrome of Hyperkalemia and Hypertension With Normal Renal Function

FNU Manas, Sneha Singh

Cureus. 2024 Jan; 16(1): e52594. Published online 2024 Jan 19. doi: 10.7759/cureus.52594

PMCID:: PMC10874887

Article PDF–83K

Select item 1085791610.

Cardiac arrest in a newborn: A case of pseudohypoaldosteronism

Kate A. Tauber, Kimberly Ermacor, James Listman

Clin Case Rep. 2024 Feb; 12(2): e8265. Published online 2024 Feb 9. doi: 10.1002/ccr3.8265

PMCID:: PMC10857916

Article PDF–709K

Select item 1084657811.

Analysis of patients presenting with serum electrolyte imbalance in terms of the differential diagnosis of pseudohypoaldosteronism

Celebi Kocaoglu, Seyma Akturk

North Clin Istanb. 2023; 10(6): 754–760. Published online 2023 Nov 6. doi: 10.14744/nci.2022.70105

PMCID:: PMC10846578

Article PDF–188K

Select item 1082287612.

Case report: Early molecular confirmation and sodium polystyrene sulfonate management of systemic pseudohypoaldosteronism type I

Einas H. Alkhatib, Deirdre Bartlett, Roopa Kanakatti Shankar, Debra Regier, Nadia Merchant

Front Endocrinol (Lausanne) 2023; 14: 1297335. Published online 2024 Jan 15. doi: 10.3389/fendo.2023.1297335

PMCID:: PMC10822876

Article PDF–294K

Select item 1079788513.

Case report: Life threatening hyponatremia in infants with urinary tract infections: two cases of type III pseudohypoaldosteronism and review of the literature

Cécile Carl, Lars Dinkelbach, Julia Mohr, Ruy Perez, Tobias Vera Lopez, Susanne Fricke-Otto, Tim Niehues

Front Pediatr. 2023; 11: 1233205. Published online 2024 Jan 5. doi: 10.3389/fped.2023.1233205

PMCID:: PMC10797885

Article PDF–1.0M

Select item 1066666714.

When the Going Gets Tough: A Case Report and Review of Calcinosis Cutis in an Infant with Pseudo-Hypoaldosteronism

Nisha Toteja, Daisy Khera, Priya Gupta, Aliza Mittal, Kuldeep Singh

Cureus. 2023 Oct; 15(10): e47579. Published online 2023 Oct 24. doi: 10.7759/cureus.47579

PMCID:: PMC10666667

Article PDF–204K

Select item 1066506815.

Pseudohypoaldosteronism type 1b in fraternal twins of a Chinese family: report of two cases and literature review

Zhen Gao, Jingjing Sun, Cheng Cai, Xiaohui Gong, Li Ma

Arch Endocrinol Metab. 2023; 67(4): e000620. Published online 2023 May 10. doi: 10.20945/2359-3997000000620

PMCID:: PMC10665068

Article PDF–1.1M

Select item 1060660816.

A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of WNK1

Ramón Peces, Carlos Peces, Laura Espinosa, Rocío Mena, Carolina Blanco, Jair Tenorio-Castaño, Pablo Lapunzina, Julián Nevado

Genes (Basel) 2023 Oct; 14(10): 1878. Published online 2023 Sep 27. doi: 10.3390/genes14101878

PMCID:: PMC10606608

Article PDF–919K

Select item 1059322617.

Unanticipated domain requirements for Drosophila Wnk kinase in vivo

Prathibha Yarikipati, Sima Jonusaite, John M. Pleinis, Carihann Dominicci Cotto, David Sanchez-Hernandez, Daryl E. Morrison, Suhani Goyal, Jeffrey Schellinger, Clothilde Pénalva, Jennifer Curtiss, Aylin R. Rodan, Andreas Jenny

PLoS Genet. 2023 Oct; 19(10): e1010975. Published online 2023 Oct 11. doi: 10.1371/journal.pgen.1010975