Bartter disease type 4B

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.