Conditions / Genetic
Bartter disease type 5
info · Genetic · ICD-10: E26.8
A Bartter disease that has_material_basis_in mutation in the MAGED2 gene on chromosome Xp11.
Signs and symptoms
- Polyhydramnios
- Hypochloremia
- Fetal polyuria
- Medullary nephrocalcinosis
- Increased circulating renin concentration
- Hyponatremia
- Hypercalciuria
- Hypokalemia
- Polyuria
- Premature birth
Also known as: BARTS5; Bartter syndrome, type 5, antenatal, transient