Statements (33)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
|
| gptkbp:affects |
kidneys
|
| gptkbp:alsoKnownAs |
Juxtaglomerular hyperplasia with hyperaldosteronism
|
| gptkbp:causedBy |
genetic mutations
defects in renal tubular transporters |
| gptkbp:characterizedBy |
hypokalemia
metabolic alkalosis hyperaldosteronism hyperreninemia |
| gptkbp:diagnosedBy |
genetic testing
blood tests urine tests |
| gptkbp:firstDescribed |
1962
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:namedAfter |
gptkb:Frederic_Bartter
|
| gptkbp:prevalence |
rare
|
| gptkbp:relatedTo |
Gitelman syndrome
|
| gptkbp:subspecies |
Type I Bartter syndrome
Type II Bartter syndrome Type III Bartter syndrome Type IV Bartter syndrome Type V Bartter syndrome |
| gptkbp:symptom |
muscle weakness
growth retardation polydipsia polyuria |
| gptkbp:treatment |
gptkb:aldosterone_antagonists
nonsteroidal anti-inflammatory drugs potassium supplements |
| gptkbp:bfsParent |
gptkb:inwardly_rectifying_potassium_channels
gptkb:loop_of_Henle |
| gptkbp:bfsLayer |
7
|
| https://www.w3.org/2000/01/rdf-schema#label |
Bartter syndrome
|