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Select item 107847291.

A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review

Yiting Lu, Xinchang Liu, Lin Sun, Di Zhang, Peng Fan, Kunqi Yang, Lin Zhang, Yaxin Liu, Xianliang Zhou

Mol Med Rep. 2024 Feb; 29(2): 19. Published online 2023 Dec 8. doi: 10.3892/mmr.2023.13142

PMCID:: PMC10784729

Abstract Article PDF–2.3M

Select item 106815482.

Liddle syndrome presenting with normal aldosterone levels: A case report

Rongrong Wang, Yan Zhang, Runzhou Pan, Rongju Zhang, Yongcai Zhao

Medicine (Baltimore) 2023 Nov 24; 102(47): e35944. Published online 2023 Nov 24. doi: 10.1097/MD.0000000000035944

PMCID:: PMC10681548

Abstract Article PDF–519K

Select item 101574203.

Neonatal presentation of a patient with Liddle syndrome, South Africa

Nicolene Steyn, Bettina Chale-Matsau, Aron B. Abera, Gertruida van Biljon, Tahir S. Pillay

Afr J Lab Med. 2023; 12(1): 1998. Published online 2023 Apr 14. doi: 10.4102/ajlm.v12i1.1998

PMCID:: PMC10157420

Abstract Article PDF–948K

Select item 92828924.

Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family

Di Zhang, Yi Qu, Xue-Qi Dong, Yi-Ting Lu, Kun-Qi Yang, Xin-Chang Liu, Peng Fan, Yu-Xiao Hu, Chun-Xue Yang, Ling-Gen Gao, Ya-Xin Liu, Xian-Liang Zhou

Front Pediatr. 2022; 10: 961964. Published online 2022 Jun 30. doi: 10.3389/fped.2022.961964

Corrects:: Front Pediatr. 2022; 10: 887214.

PMCID:: PMC9282892

Correction PDF–83K

Select item 91709205.

Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family

Di Zhang, Yi Qu, Xue-Qi Dong, Yi-Ting Lu, Kun-Qi Yang, Xin-Chang Liu, Peng Fan, Yu-Xiao Hu, Chun-Xue Yang, Ling-Gen Gao, Ya-Xin Liu, Xian-Liang Zhou

Front Pediatr. 2022; 10: 887214. Published online 2022 May 24. doi: 10.3389/fped.2022.887214

Correction in:: Front Pediatr. 2022; 10: 961964.

PMCID:: PMC9170920

Abstract Article PDF–1.0M

Select item 88164706.

High Prevalence of Liddle Syndrome Phenotype Among Hypertensive US Veterans in Northwest Louisiana

Mihály Tapolyai, Aşkin Uysal, Neville R. Dossabhoy, Lajos Zsom, Tibor Szarvas, Zsolt Lengvárszky, Tibor Fülöp

J Clin Hypertens (Greenwich) 2010 Nov; 12(11): 856–860. Published online 2010 Aug 20. doi: 10.1111/j.1751-7176.2010.00359.x

PMCID:: PMC8816470

Abstract Article PDF–127K

Select item 80318487.

Prevalence of Liddle Syndrome Among Young Hypertension Patients of Undetermined Cause in a Chinese Population

Lin‐Ping Wang, Kun‐Qi Yang, Xiong‐Jing Jiang, Hai‐Ying Wu, Hui‐Min Zhang, Yu‐Bao Zou, Lei Song, Jin Bian, Ru‐Tai Hui, Ya‐Xin Liu, Xian‐Liang Zhou

J Clin Hypertens (Greenwich) 2015 Nov; 17(11): 902–907. Published online 2015 Jun 15. doi: 10.1111/jch.12598

PMCID:: PMC8031848

Abstract Article PDF–114K

Select item 80309338.

Liddle syndrome: clinical and genetic profiles

Yunying Cui, Anli Tong, Jun Jiang, Fen Wang, Chunyan Li

J Clin Hypertens (Greenwich) 2017 May; 19(5): 524–529. Published online 2016 Nov 29. doi: 10.1111/jch.12949

PMCID:: PMC8030933

Abstract Article PDF–476K

Select item 79241639.

Liddle Syndrome due to a Novel c.1713 Deletion in the Epithelial Sodium Channel β-Subunit in a Normotensive Adolescent

Raven K. Brower, Ida A. Ghlichloo, Venus Shabgahi, Daniel Elsholz, Ram K. Menon, Arpita K. Vyas

AACE Clin Case Rep. 2021 Jan-Feb; 7(1): 65–68. Published online 2020 Dec 28. doi: 10.1016/j.aace.2020.11.017

PMCID:: PMC7924163

Abstract Article PDF–877K

Select item 736816810.

Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension

Peng Fan, Xiao-Cheng Pan, Di Zhang, Kun-Qi Yang, Ying Zhang, Tao Tian, Fang Luo, Wen-Jun Ma, Ya-Xin Liu, Lin-Ping Wang, Hui-Min Zhang, Lei Song, Jun Cai, Xian-Liang Zhou

Am J Hypertens. 2020 Jul; 33(7): 670–675. Published online 2020 Mar 12. doi: 10.1093/ajh/hpaa037

PMCID:: PMC7368168

Abstract Article PDF–456K

Select item 730354211.

A case report of three children with secondary hypertension caused by Liddle syndrome

Zheyi Teoh, Siddharth Shah

Clin Nephrol Case Stud. 2020; 8: 37–40. Published online 2020 May 29. doi: 10.5414/CNCS109972

PMCID:: PMC7303542

Abstract Article PDF–698K

Select item 681546312.

Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium channel (ENaC) in family from Russia: a case report

Anastasiya A. Kozina, Tatiana A. Trofimova, Elena G. Okuneva, Natalia V. Baryshnikova, Varvara A. Obuhova, Anna Yu. Krasnenko, Kirill Yu. Tsukanov, Olesya I. Klimchuk, Ekaterina I. Surkova, Peter A. Shatalov, Valery V. Ilinsky

BMC Nephrol. 2019; 20: 389. Published online 2019 Oct 26. doi: 10.1186/s12882-019-1579-4

PMCID:: PMC6815463

Abstract Article PDF–1005K

Select item 663678913.

A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia

Peng Fan, Yu-Mo Zhao, Di Zhang, Ying Liao, Kun-Qi Yang, Tao Tian, Ying Lou, Fang Luo, Wen-Jun Ma, Hui-Min Zhang, Lei Song, Jun Cai, Ya-Xin Liu, Xian-Liang Zhou

Am J Hypertens. 2019 Jul; 32(8): 752–758. Published online 2019 Apr 12. doi: 10.1093/ajh/hpz053

PMCID:: PMC6636789

Abstract Article PDF–2.5M

Select item 631146314.

Liddle syndrome misdiagnosed as primary aldosteronism resulting from a novel frameshift mutation of SCNN1B

Peng Fan, Chao-Xia Lu, Di Zhang, Kun-Qi Yang, Pei-Pei Lu, Ying Zhang, Xu Meng, Su-Fang Hao, Fang Luo, Ya-Xin Liu, Hui-Min Zhang, Lei Song, Jun Cai, Xue Zhang, Xian-Liang Zhou

Endocr Connect. 2018 Dec; 7(12): 1528–1534. Published online 2018 Nov 28. doi: 10.1530/EC-18-0484

PMCID:: PMC6311463

Abstract Article PDF–741K

Select item 587767315.

Liddle Syndrome: Review of the Literature and Description of a New Case

Martina Tetti, Silvia Monticone, Jacopo Burrello, Patrizia Matarazzo, Franco Veglio, Barbara Pasini, Xavier Jeunemaitre, Paolo Mulatero

Int J Mol Sci. 2018 Mar; 19(3): 812. Published online 2018 Mar 11. doi: 10.3390/ijms19030812

PMCID:: PMC5877673

Abstract Article PDF–1.1M

Select item 576712116.

Three reportedly unrelated families with Liddle’s syndrome inherited from a common ancestor

Luca Pagani, Yoan Diekmann, Marco Sazzini, Sara De Fanti, Maurizio Rondinelli, Enrico Farnetti, Bruno Casali, Amelia Caretto, Francesca Novara, Orsetta Zuffardi, Paolo Garagnani, Franco Mantero, Mark G. Thomas, Donata Luiselli, Ermanno Rossi

Hypertension. Author manuscript; available in PMC 2019 Feb 1.

Published in final edited form as: Hypertension. 2018 Feb; 71(2): 273–279. Published online 2017 Dec 11. doi: 10.1161/HYPERTENSIONAHA.117.10491

PMCID:: PMC5767121

Abstract Article PDF–684K

Select item 566127517.

A Missense Mutation in the Extracellular Domain of αENaC Causes Liddle Syndrome

Mahdi Salih, Ivan Gautschi, Miguel X. van Bemmelen, Michael Di Benedetto, Alice S. Brooks, Dorien Lugtenberg, Laurent Schild, Ewout J. Hoorn

J Am Soc Nephrol. 2017 Nov; 28(11): 3291–3299. Published online 2017 Jul 14. doi: 10.1681/ASN.2016111163

PMCID:: PMC5661275

Abstract Article

Select item 545374218.

Liddle Syndrome in Association with Aortic Dissection

Aamer Abbass, Jason D'Souza, Sameen Khalid, FNU Asad-Ur-Rahman, Joseph Limback, Jeremy Burt, Rajesh Shah

Cureus. 2017 May; 9(5): e1225. Published online 2017 May 4. doi: 10.7759/cureus.1225

PMCID:: PMC5453742

Abstract Article PDF–1.6M

Select item 537047719.

Management of Liddle Syndrome in Pregnancy: A Case Report and Literature Review

Michael Awadalla, Manasi Patwardhan, Adham Alsamsam, Nashat Imran

Case Rep Obstet Gynecol. 2017; 2017: 6279460. Published online 2017 Mar 15. doi: 10.1155/2017/6279460

PMCID:: PMC5370477

Abstract Article PDF–639K

Select item 511100920.

Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome

Linda M. Polfus, Eric Boerwinkle, Richard A. Gibbs, Ginger Metcalf, Donna Muzny, Narayanan Veeraraghavan, Megan Grove, Sanjay Shete, Stephanie Wallace, Dianna Milewicz, Neil Hanchard, James R. Lupski, Syed Shahrukh Hashmi, Monesha Gupta-Malhotra

Cold Spring Harb Mol Case Stud. 2016 Nov; 2(6): a001255. doi: 10.1101/mcs.a001255