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Descriptor English: Bartter Syndrome
Descriptor Spanish: Síndrome de Bartter
Descriptor síndrome de Bartter
Scope note: Grupo de trastornos causados por reabsorción defectuosa de sal en la porción ascendente del ASA DE HENLE. Se caracteriza por intensa pérdida de sal, HIPOPOTASEMIA, HIPERCALCIURIA, ALCALOSIS metabólica e HIPERALDOSTERONISMO hiperreninémico sin HIPERTENSIÓN. Hay varios subtipos que son el resultado de mutaciones autosómicas recesivas en los genes que codifican los COTRANSPORTADORES DE SODIO-POTASIO-CLORURO.
Descriptor Portuguese: Síndrome de Bartter
Descriptor French: Syndrome de Bartter
Entry term(s): Aldosteronism with Hyperplasia of the Adrenal Cortex
Bartter Disease
Bartter's Disease
Bartter's Syndrome
Bartters Disease
Bartters Syndrome
Juxtaglomerular Hyperplasia with Secondary Aldosteronism
Syndrome, Bartter
Syndrome, Bartter's
Tree number(s): C12.050.351.968.419.815.279
C12.200.777.419.815.279
C12.950.419.815.279
C19.053.800.604.249
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D001477
Scope note: 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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 2005; see BARTTER'S DISEASE 1991-2004, see HYPERALDOSTERONISM 1975-1990
History Note: 2005 (1975)
Related: Sodium-Potassium-Chloride Symporters MeSH
DeCS ID: 1498
Unique ID: D001477
NLM Classification: WK 770
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1991/01/01
Date of Entry: 1999/01/01
Revision Date: 2013/07/08
Bartter Syndrome - Preferred
Concept UI M0002194
Scope note 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.
Preferred term Bartter Syndrome
Entry term(s) Aldosteronism with Hyperplasia of the Adrenal Cortex
Bartter Disease
Bartter's Disease
Bartter's Syndrome
Bartters Disease
Bartters Syndrome
Juxtaglomerular Hyperplasia with Secondary Aldosteronism
Syndrome, Bartter
Syndrome, Bartter's



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