Search on: LAURENCE-MOON SYNDROME 
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Descriptor English:   Laurence-Moon Syndrome 
Descriptor Spanish:   Síndrome de Laurence-Moon 
Descriptor Portuguese:   Síndrome de Laurence-Moon 
Synonyms English:   Laurence-Moon-Biedl Syndrome  
Tree Number:   C10.228.140.617.500
C16.131.077.509
Definition English:   An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY. This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity. (From N Engl J Med. 1989 Oct 12;321(15):1002-9) 
Indexing Annotation English:   note X ref: do not confuse with LAURENCE-MOON-BARDET-BIEDL SYNDROME see BARDET-BIEDL SYNDROME
See Related English:   Intellectual Disability
 
History Note English:   2000 (1966) 
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:   8028 
Unique Identifier:   D007849 

Occurrence in VHL: 		 

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