Bartter Syndrome [Bartterův syndrom]

topical
20
Terms

Aldosteronism with Hyperplasia of the Adrenal Cortex
Bartter Disease
Bartter's Disease
Bartter's Syndrome
Juxtaglomerular Hyperplasia with Secondary Aldosteronism

Persistent link   https://www.medvik.cz/link/D001477
Definition

A group of disorders caused by defective salt reabsorption in the ascending LOOP OF HENLE. It is characterized by severe salt-wasting, HYPOKALEMIA; HYPERCALCIURIA; metabolic ALKALOSIS, and hyper-reninemic HYPERALDOSTERONISM without HYPERTENSION. There are several subtypes including ones due to mutations in the renal specific SODIUM-POTASSIUM-CHLORIDE SYMPORTERS.

DUI
D001477 MeSH Browser
CUI
M0002194
History note
2005 (1975)
Public note
2005; see BARTTER'S DISEASE 1991-2004, see HYPERALDOSTERONISM 1975-1990

C Diseases
C12.050.351.968 Urologic Diseases 836
C12.050.351.968.419 Kidney Diseases 3 067
C12.050.351.968.419.815 Renal Tubular Transport, Inborn Errors 36
C12.050.351.968.419.815.093 Acidosis, Renal Tubular 59
C12.050.351.968.419.815.279 Bartter Syndrome 20
C12.050.351.968.419.815.364 Dent Disease 1
C12.050.351.968.419.815.450 Fanconi Syndrome 23
C12.050.351.968.419.815.491 Gitelman Syndrome 18
C12.050.351.968.419.815.532 Glycosuria, Renal 36
C12.050.351.968.419.815.647 Hypophosphatemia, Familial 12
C12.050.351.968.419.815.683 Liddle Syndrome 4
C12.050.351.968.419.815.720 Oculocerebrorenal Syndrome 9
C12.050.351.968.419.815.770 Pseudohypoaldosteronism 10
C12.050.351.968.419.815.885 Renal Aminoacidurias 27
C12.200.777 Urologic Diseases 836
C12.200.777.419 Kidney Diseases 3 067
C12.200.777.419.815.093 Acidosis, Renal Tubular 59
C12.200.777.419.815.279 Bartter Syndrome 20
C12.200.777.419.815.364 Dent Disease 1
C12.200.777.419.815.450 Fanconi Syndrome 23
C12.200.777.419.815.491 Gitelman Syndrome 18
C12.200.777.419.815.532 Glycosuria, Renal 36
C12.200.777.419.815.647 Hypophosphatemia, Familial 12
C12.200.777.419.815.683 Liddle Syndrome 4
C12.200.777.419.815.720 Oculocerebrorenal Syndrome 9
C12.200.777.419.815.770 Pseudohypoaldosteronism 10
C12.200.777.419.815.885 Renal Aminoacidurias 27
C12.950.419 Kidney Diseases 3 067
C12.950.419.815.093 Acidosis, Renal Tubular 59
C12.950.419.815.279 Bartter Syndrome 20
C12.950.419.815.364 Dent Disease 1
C12.950.419.815.450 Fanconi Syndrome 23
C12.950.419.815.491 Gitelman Syndrome 18
C12.950.419.815.532 Glycosuria, Renal 36
C12.950.419.815.647 Hypophosphatemia, Familial 12
C12.950.419.815.683 Liddle Syndrome 4
C12.950.419.815.720 Oculocerebrorenal Syndrome 9
C12.950.419.815.770 Pseudohypoaldosteronism 10
C12.950.419.815.885 Renal Aminoacidurias 27
C19.053.800.604 Hyperaldosteronism 325
C19.053.800.604.249 Bartter Syndrome 20

Bartter Syndrome, Type 3, with Hypocalciuria Disease MeSH Browser

Bartter Syndrome, Type 4A Disease MeSH Browser

Bartter Syndrome, Type 4b Disease MeSH Browser

Bartter syndrome, antenatal , type 2 Disease MeSH Browser

Bartter syndrome, antenatal type 1 Disease MeSH Browser

Bartter syndrome, type 3 Disease MeSH Browser

Hypocalcemia, Autosomal Dominant, with Bartter Syndrome Disease MeSH Browser

Sensorineural Deafness With Mild Renal Dysfunction Disease MeSH Browser