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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.

external link
2.

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

external link
3.

OMIM.ORG article

Omim 300971 external link
Update: Aug. 14, 2020
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