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.

Systematic

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
MAGED2

References:

1.

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

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2.

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

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Update: Sept. 26, 2018