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
Syndrome, Liddle  
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
DG diagnostic imaging 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 RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   53532 
Unique Identifier:   D056929 

Occurrence in VHL: 		 

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DeCS