Statements (34)
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
|
https://www.w3.org/2000/01/rdf-schema#label |
Bartter syndrome
|
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 gptkb:Frederic_Bartter |
gptkbp:bfsLayer |
7
|