Search
Descriptor English: Liddle Syndrome
Descriptor Spanish: Síndrome de Liddle
Descriptor síndrome de Liddle
Entry term(s) pseudoaldosteronismo
Scope note: Pseudoaldosteronismo familiar caracterizado por la herencia autosómica recesiva de hipertensión con HIPOCALEMIA, ALCALOSIS, y disminución de los niveles de RENINA y ALDOSTERONA. Este cuadro se debe a mutaciones en las subunidades beta y gamma de los CANALES DE SODIO EPITELIALES. Diversas mutaciones en las mismas subunidades de los CANALES DE SODIO EPITELIALES pueden causar PSEUDOHIPOALDOSTERONISMO TIPO I AUTOSÓMICO DOMINANTE.
Descriptor Portuguese: Síndrome de Liddle
Descriptor French: Syndrome de Liddle
Entry term(s): Pseudoaldosteronism
Syndrome, Liddle
Tree number(s): C12.050.351.968.419.815.683
C12.200.777.419.815.683
C12.950.419.815.683
C16.320.831.698
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D056929
Scope note: Familial pseudoaldosteronism characterized by autosomal dominant inheritance of hypertension with HYPOKALEMIA; ALKALOSIS; RENIN and ALDOSTERONE level decreases. It is caused by mutations in EPITHELIAL SODIUM CHANNELS beta and gamma subunits. Different mutations in the same EPITHELIAL SODIUM CHANNELS subunits can cause PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT.
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: 2010
History Note: 2010
Related: Epithelial Sodium Channels MeSH
DeCS ID: 53532
Unique ID: D056929
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2010/01/01
Date of Entry: 2009/07/06
Revision Date: 2012/07/03
Liddle Syndrome - Preferred
Concept UI M0533461
Scope note Familial pseudoaldosteronism characterized by autosomal dominant inheritance of hypertension with HYPOKALEMIA; ALKALOSIS; RENIN and ALDOSTERONE level decreases. It is caused by mutations in EPITHELIAL SODIUM CHANNELS beta and gamma subunits. Different mutations in the same EPITHELIAL SODIUM CHANNELS subunits can cause PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT.
Preferred term Liddle Syndrome
Entry term(s) Pseudoaldosteronism
Syndrome, Liddle



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.

Go to survey