Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Transient antenatal Bartter syndrome

Bartter syndrome type 5 is an x-linked recessive disorder caused by mutations of the MAGED2 gene. It is characterized by antenatal manifestation with polyhydramnios and recovery soon after birth.


Bartter syndrome
Antenatal Bartter syndrome type 1
Antenatal Bartter syndrome type 2
Classic Bartter syndrome
Hypercalciuric hypocalcemia 1
Hypercalciuric hypocalcemia 2
Infantile Bartter syndrome with deafness type 4
Transient antenatal Bartter syndrome



Reinalter S et. al. (1998) Neonatal Bartter syndrome: spontaneous resolution of all signs and symptoms.


Laghmani K et. al. (2016) Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations.

Update: Sept. 26, 2018