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A form of Bartter syndrome characterized by maternal polyhydramnios, premature delivery, salt loss, polyuria and sensorineural deafness, associated with hypokalemic and hypochloremic metabolic alkalosis, increased levels of plasma renin and aldosterone, and low to normal blood pressure. Urinary calcium excretion rates are variable, and nephrocalcinosis is typically absent.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for Bartter syndrome type 4.
7 publications have been identified in PubMed for Bartter syndrome type 4. Research spans Case Report / Case Series (57%), Other (14%), and Review / Meta-Analysis (14%).
Swetha J (2026). [PMID: 42166039](https://pubmed.ncbi.nlm.nih.gov/42166039/). *Pediatr Nephrol*. [Review / Meta-Analysis]
Bonomo JH (2026). [PMID: 41821755](https://pubmed.ncbi.nlm.nih.gov/41821755/). *Biomed Rep*. [Basic Science / Preclinical]
Vadher A (2025). [PMID: 41472911](https://pubmed.ncbi.nlm.nih.gov/41472911/). *Case Rep Nephrol*. [Case Report / Case Series]
Badr KM (2025). [PMID: 40589384](https://pubmed.ncbi.nlm.nih.gov/40589384/). *Sci Prog*. [Case Report / Case Series]
Mathew GG (2025). [PMID: 39992172](https://pubmed.ncbi.nlm.nih.gov/39992172/). *J Bras Nefrol*. [Other]
Oweidat M (2025). [PMID: 40612195](https://pubmed.ncbi.nlm.nih.gov/40612195/). *Sage Open Pediatr*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 1:00 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about Bartter syndrome type 4
Das A (2024). [PMID: 39588405](https://pubmed.ncbi.nlm.nih.gov/39588405/). *Cureus*. [Case Report / Case Series]
AI-curated news mentioning Bartter syndrome type 4
Updated Jul 8, 2026
A new treatment for children aged 2 or older with sickle cell disease has been approved by the U.S. Food & Drug Administration. In a press release on Wednesday, the FDA announced it had approved Casgevy, the first gene therapy for children with sickle cell disease. (NewsNation) — A new treatment for children aged 2 or older with sickle cell disease has been approved by the Food & Drug Administration (FDA). In a Wednesday news release, the FDA announced it had approved Casgevy, the first gene therapy for children with the disease. “Casgevy is a gene therapy consisting of the patient’s own (autologous) hematopoietic (blood) stem cells, administered as a one-time single dose for intravenous infusion,” the release noted. “Pediatric patients as young as 2 years of age can now access a critical additional treatment option to treat these debilitating, life-threatening diseases,” Karim Mikhail, the acting director of the Center for Biologics Evaluation and Research, wrote. “These disorders carry a heavy burden for children and their families, affecting growth, development, and long-term health in profound ways,” Megha Kaushal, acting deputy director of the Office of Therapeutic Products in CBER, said in the release.