Literature DB >> 29229168

Monogenic Hypertension in Children: A Review With Emphasis on Genetics.

Anjali Aggarwal1, David Rodriguez-Buritica2.   

Abstract

Hypertension (HT) is a public health problem in children particularly related to the epidemic of overweight and obesity. Monogenic forms of HT are important in the differential diagnosis in children presenting with severe or refractory HT, who have a family history of early-onset HT, unusual physical examination findings, and/or characteristic hormonal and biochemical abnormalities. Most genetic defects in these disorders ultimately result in increased sodium transport in the distal nephron resulting in volume expansion and HT. Genetic testing, which is increasingly available, has diagnostic, therapeutic, and predictive implications for families affected by these rare conditions.
Copyright © 2017. Published by Elsevier Inc.

Entities:  

Keywords:  Etiology; Genes; Hypertension; Pediatrics; Syndrome

Mesh:

Year:  2017        PMID: 29229168     DOI: 10.1053/j.ackd.2017.09.006

Source DB:  PubMed          Journal:  Adv Chronic Kidney Dis        ISSN: 1548-5595            Impact factor:   3.620


  1 in total

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

Authors:  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
Journal:  Am J Hypertens       Date:  2020-07-18       Impact factor: 2.689

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.