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.
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.[^]