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About 98 results

ALLMedicine™ Liddle Syndrome Center

Research & Reviews  49 results

Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused b...
https://doi.org/10.1159/000507580
Kidney & Blood Pressure Research; Fan P, Zhang D et. al.

Jul 22nd, 2020 - Liddle syndrome (LS), an autosomal dominant and inherited monogenic hypertension syndrome caused by pathogenic mutations in the epithelial sodium channel (ENaC) genes SCNN1A, SCNN1B, and SCNN1G. This study was designed to identify a novel SCNN1B m...

Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Char...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368168
American Journal of Hypertension; Fan P, Pan XC et. al.

Mar 12th, 2020 - Liddle syndrome (LS), an autosomal dominant disorder, is a common monogenic hypertension in pediatrics. In this study, we reported a novel SCNN1G variant in a Chinese family with pediatric LS, and conduct a systematic review of epithelial sodium c...

Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium chann...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815463
BMC Nephrology; Kozina AA, Trofimova TA et. al.

Oct 27th, 2019 - Liddle syndrome is a monogenic disease with autosomal dominant inheritance. Basic characteristics of this disease are hypertension, reduced concentration of aldosterone and renin activity, as well as increased excretion of potassium leading to low...

A Novel Association of Martorell Ulcer With Liddle Syndrome.
https://doi.org/10.1097/01.ASW.0000582616.30031.19
Advances in Skin & Wound Care; Malphrus E, Couch K et. al.

Oct 18th, 2019 - Pseudohyperaldosteronism, or Liddle syndrome, is a rare, autosomal dominant condition characterized by early-onset hypertension, often associated with hypokalemia and metabolic alkalosis. Martorell hypertensive ischemic leg ulcer is a rare, underd...

Truncated Epithelial Sodium Channel β Subunit Responsible for Liddle Syndrome in a Chin...
https://doi.org/10.1159/000500919
Kidney & Blood Pressure Research; Fan P, Lu CX et. al.

Aug 22nd, 2019 - Liddle syndrome (LS) is a rare autosomal dominant disease caused by mutations in genes coding for epithelial sodium channel (ENaC) subunits. The aim of this study was to identify the mutation responsible for the LS in an extended Chinese family. D...

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Clinicaltrials.gov  49 results

Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused b...
https://doi.org/10.1159/000507580
Kidney & Blood Pressure Research; Fan P, Zhang D et. al.

Jul 22nd, 2020 - Liddle syndrome (LS), an autosomal dominant and inherited monogenic hypertension syndrome caused by pathogenic mutations in the epithelial sodium channel (ENaC) genes SCNN1A, SCNN1B, and SCNN1G. This study was designed to identify a novel SCNN1B m...

Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Char...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368168
American Journal of Hypertension; Fan P, Pan XC et. al.

Mar 12th, 2020 - Liddle syndrome (LS), an autosomal dominant disorder, is a common monogenic hypertension in pediatrics. In this study, we reported a novel SCNN1G variant in a Chinese family with pediatric LS, and conduct a systematic review of epithelial sodium c...

Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium chann...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815463
BMC Nephrology; Kozina AA, Trofimova TA et. al.

Oct 27th, 2019 - Liddle syndrome is a monogenic disease with autosomal dominant inheritance. Basic characteristics of this disease are hypertension, reduced concentration of aldosterone and renin activity, as well as increased excretion of potassium leading to low...

A Novel Association of Martorell Ulcer With Liddle Syndrome.
https://doi.org/10.1097/01.ASW.0000582616.30031.19
Advances in Skin & Wound Care; Malphrus E, Couch K et. al.

Oct 18th, 2019 - Pseudohyperaldosteronism, or Liddle syndrome, is a rare, autosomal dominant condition characterized by early-onset hypertension, often associated with hypokalemia and metabolic alkalosis. Martorell hypertensive ischemic leg ulcer is a rare, underd...

Truncated Epithelial Sodium Channel β Subunit Responsible for Liddle Syndrome in a Chin...
https://doi.org/10.1159/000500919
Kidney & Blood Pressure Research; Fan P, Lu CX et. al.

Aug 22nd, 2019 - Liddle syndrome (LS) is a rare autosomal dominant disease caused by mutations in genes coding for epithelial sodium channel (ENaC) subunits. The aim of this study was to identify the mutation responsible for the LS in an extended Chinese family. D...

see more →