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Page 1
[Liddle syndrome].
Mareš Š, Filipovský J. Mareš Š, et al. Vnitr Lek. 2022 Winter;68(E-8):8-11. doi: 10.36290/vnl.2022.115. Vnitr Lek. 2022. PMID: 36575060 Czech.
Liddle syndrome is an inherited form of arterial hypertension with autosomal dominant pattern of inheritance. ...Phenotypic variability makes it difficult to identify patients with Liddle syndrome, often resulting in misdiagnosis and severe complicatio …
Liddle syndrome is an inherited form of arterial hypertension with autosomal dominant pattern of inheritance. ...Phenotypic va …
Liddle's syndrome.
Palmer BF, Alpern RJ. Palmer BF, et al. Am J Med. 1998 Mar;104(3):301-9. doi: 10.1016/s0002-9343(98)00018-7. Am J Med. 1998. PMID: 9552093 Review. No abstract available.
Liddle Syndrome (Pseudohyperaldosteronism).
Mubarik A, Anastasopoulou C, Aeddula NR. Mubarik A, et al. 2024 Mar 1. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2024 Mar 1. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 30725596 Free Books & Documents.
Liddle syndrome is one of the rare causes of resistant hypertension that usually presents in early childhood, but some are not detected until well into adulthood. First explained by Grant Liddle et al in 1963, this syndrome is characterized by a primar …
Liddle syndrome is one of the rare causes of resistant hypertension that usually presents in early childhood, but some are not …
Liddle's Syndrome.
Aziz DA, Memon F, Rahman A, Ali M. Aziz DA, et al. J Ayub Med Coll Abbottabad. 2016 Oct-Dec;28(4):809-811. J Ayub Med Coll Abbottabad. 2016. PMID: 28586600 Free article.
Paediatric Hypertension is one of the important clinical finding in a child with certain clinical syndrome. We are presenting a case of a 10 month old child presenting with hypertension and hypokalaemia, after excluding all identifiable causes and her positive response to …
Paediatric Hypertension is one of the important clinical finding in a child with certain clinical syndrome. We are presenting a case …
Liddle Syndrome with a SCNN1A Mutation: A Case Report and Literature Review.
Tian J, Xiang F, Wang L, Wu X, Shao L, Ma L, Fang C. Tian J, et al. Kidney Blood Press Res. 2024;49(1):831-838. doi: 10.1159/000540522. Epub 2024 Sep 5. Kidney Blood Press Res. 2024. PMID: 39236685 Free article. Review.
The aetiology of Liddle syndrome is missense or frameshift mutations in the SCNN1A, SCNN1B, or SCNN1G genes, which encode for the epithelial sodium channel subunits. ...CONCLUSION: A middle-aged patient with Liddle syndrome was diagnosed. A new point m …
The aetiology of Liddle syndrome is missense or frameshift mutations in the SCNN1A, SCNN1B, or SCNN1G genes, which encode for …
Liddle syndrome: A case report.
Jin Y, Qiu W, Yao J. Jin Y, et al. Med Clin (Barc). 2021 Jun 16:S0025-7753(21)00299-2. doi: 10.1016/j.medcli.2021.03.035. Online ahead of print. Med Clin (Barc). 2021. PMID: 34147249 English, Spanish.
INTRODUCTION: Liddle syndrome is an autosomal dominant hereditary disease caused by a single gene mutation. ...DISCUSSION: The patient is an atypical case of Liddle syndrome; genetic analysis is helpful and essential for diagnosis....
INTRODUCTION: Liddle syndrome is an autosomal dominant hereditary disease caused by a single gene mutation. ...DISCUSSION: The …
Reverse Phenotypes of Patients with Genetically Confirmed Liddle Syndrome.
Granhøj J, Nøhr TK, Hinrichs GR, Rasmussen M, Svenningsen P. Granhøj J, et al. Clin J Am Soc Nephrol. 2024 May 1;19(5):610-619. doi: 10.2215/CJN.0000000000000430. Epub 2024 Jan 24. Clin J Am Soc Nephrol. 2024. PMID: 38265765 Free PMC article.
In this study, we used a reverse phenotyping approach to investigate the Liddle syndrome phenotypic spectrum and genotype-phenotype correlations. METHODS: Pubmed, Embase, Scopus, and the Human Gene Mutation Database were searched for articles reporting Liddle …
In this study, we used a reverse phenotyping approach to investigate the Liddle syndrome phenotypic spectrum and genotype-phen …
Molecular genetics of Liddle's syndrome.
Yang KQ, Xiao Y, Tian T, Gao LG, Zhou XL. Yang KQ, et al. Clin Chim Acta. 2014 Sep 25;436:202-6. doi: 10.1016/j.cca.2014.05.015. Epub 2014 May 29. Clin Chim Acta. 2014. PMID: 24882431 Review.
Liddle's syndrome, an autosomal dominant form of monogenic hypertension, is characterized by salt-sensitive hypertension with early penetrance, hypokalemia, metabolic alkalosis, suppression of plasma rennin activity and aldosterone secretion, and a clear-cut respons …
Liddle's syndrome, an autosomal dominant form of monogenic hypertension, is characterized by salt-sensitive hypertension with …
Liddle Syndrome: Review of the Literature and Description of a New Case.
Tetti M, Monticone S, Burrello J, Matarazzo P, Veglio F, Pasini B, Jeunemaitre X, Mulatero P. Tetti M, et al. Int J Mol Sci. 2018 Mar 11;19(3):812. doi: 10.3390/ijms19030812. Int J Mol Sci. 2018. PMID: 29534496 Free PMC article. Review.
Liddle syndrome is an inherited form of low-renin hypertension, transmitted with an autosomal dominant pattern. The molecular basis of Liddle syndrome resides in germline mutations of the SCNN1A, SCNN1B and SCNN1G genes, encoding the alpha, beta, and g …
Liddle syndrome is an inherited form of low-renin hypertension, transmitted with an autosomal dominant pattern. The molecular …
Liddle's syndrome mechanisms, diagnosis and management.
Enslow BT, Stockand JD, Berman JM. Enslow BT, et al. Integr Blood Press Control. 2019 Sep 3;12:13-22. doi: 10.2147/IBPC.S188869. eCollection 2019. Integr Blood Press Control. 2019. PMID: 31564964 Free PMC article.
This review examines the clinical features of Liddle's syndrome, the differential diagnosis of Liddle's syndrome and differentiation from other genetic diseases with similar phenotype, and what is currently known about the population-level prevalence o …
This review examines the clinical features of Liddle's syndrome, the differential diagnosis of Liddle's syndrome …
652 results

Searches related to "liddle syndrome"