Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance
Bartter syndrome (BS) is a rare tubulopathy that causes polyuria, hypokalemia, hypochloremic metabolic alkalosis, and normotensive hyperreninemic hyperaldosteronism. It is characterized by locus, clinical, and allelic heterogeneity. Types 1-4 of BS are inherited according to an autosomal recessive p...
Saved in:
Main Authors: | Laura Florea (Author), Lavinia Caba (Author), Eusebiu Vlad Gorduza (Author) |
---|---|
Format: | Book |
Published: |
Frontiers Media S.A.,
2022-06-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Gitelman's and Bartter's syndromes: from genetics to the molecular basis of hypertension and more
by: Verdiana Ravarotto, et al.
Published: (2022) -
Loop tubulopathies: Bartter's syndrome
by: Alexander A. Baranov, et al.
Published: (2019) -
Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review
by: Eva-Cristiana Gavril, et al.
Published: (2021) -
Rare Case of First Permanent Molar Primary Failure of Eruption with Agenesis of Premolars
by: Arina Vinereanu, et al.
Published: (2024) -
Pediatric Bartter syndrome: The therapeutic challenge
by: Aamir Jalal Al Mosawi
Published: (2020)