Bartter disease type 4B

MONDO:0000909

A Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes.

Also known as: BARTS4B, Bartter disease type 4B, Bartter syndrome, type 4B, Bartter syndrome, infantile, with sensorineural deafness, Bartter syndrome, type 4B, neonatal, with sensorineural deafness

1 clinical trial for this condition and its sub-types, 0 tagged with Bartter disease type 4B itself.

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Where it sits in the disease tree

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↑ Bartter syndrome type 4 (0)

Including sub-types (1) Tagged with Bartter disease type 4B (0)

Trials to join now! 1

Could a diabetes drug protect kidneys in children with genetic disease?

Disease control Recruiting now

This study tests whether adding dapagliflozin (a diabetes drug) to standard care reduces protein leakage in the urine of children with hereditary kidney diseases. About 44 children will receive either dapagliflozin plus standard care or standard care alone for 12 weeks, then swit…

Phase 3 • Sponsor: Children's Hospital of Fudan University • Aim: Disease control

Last updated Jul 08, 2026 00:00 UTC

Bartter disease type 4B

Where it sits in the disease tree

Could a diabetes drug protect kidneys in children with genetic disease?