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.
1. |
Reinalter S et al. (1998) Neonatal Bartter syndrome: spontaneous resolution of all signs and symptoms. |
2. |
Laghmani K et al. (2016) Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations. |
3. |
OMIM.ORG article Omim 300971 |