Search on: LIDDLE SYNDROME 
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Descriptor English:   Liddle Syndrome 
Descriptor Spanish:   Síndrome de Liddle 
Descriptor Portuguese:   Síndrome de Liddle 
Synonyms English:   Pseudoaldosteronism  
Tree Number:   C12.777.419.815.683
C13.351.968.419.815.683
C16.320.565.861.698
C18.452.648.861.698
Definition English:   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. 
See Related English:   Epithelial Sodium Channels
 
History Note English:   2010 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RA radiography RI radionuclide imaging
RT radiotherapy RH rehabilitation
SU surgery TH therapy
US ultrasonography UR urine
VE veterinary VI virology
Record Number:   53532 
Unique Identifier:   D056929 

Occurrence in VHL: 		 

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