Pesquisa sobre: SMITH-LEMLI-OPITZ SYNDROME 
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Descritor Inglês:   Smith-Lemli-Opitz Syndrome 
Descritor Espanhol:   Síndrome de Smith-Lemli-Opitz 
Descritor Português:   Síndrome de Smith-Lemli-Opitz 
Sinônimos Inglês:   7-Dehydrocholesterol Reductase Deficiencies
7-Dehydrocholesterol Reductase Deficiency
Acrodysgenital Syndrome, Lethal
Acrodysgenital Syndromes, Lethal
Deficiencies, 7-Dehydrocholesterol Reductase
Deficiency, 7-Dehydrocholesterol Reductase
Hyperotosis Corticalis Generalisata Familiaris
Lethal Acrodysgenital Syndrome
Lethal Acrodysgenital Syndromes
Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobar Lung
RSH SLO Syndrome
RSH Syndrome
RSH Syndromes
RSH-SLO Syndrome
RSH-SLO Syndromes
Reductase Deficiencies, 7-Dehydrocholesterol
Reductase Deficiency, 7-Dehydrocholesterol
Rutledge Friedman Harrod Syndrome
Rutledge Lethal Multiple Congenital Anomaly Syndrome
SLO Syndrome
SLO Syndromes
Smith Lemli Opitz Syndrome
Smith Lemli Opitz Syndrome, Type 2
Smith Lemli Opitz Syndrome, Type I
Smith Lemli Opitz Syndrome, Type II
Smith Lemli Opitz syndrome, type 1
Smith-Lemli-Opitz Syndrome, Type 1
Smith-Lemli-Opitz Syndrome, Type 2
Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type II
Syndrome, Lethal Acrodysgenital
Syndrome, RSH
Syndrome, SLO
Syndromes, RSH
Syndromes, SLO  
Categoria:   C16.131.077.860
C16.320.565.398.850
C16.320.565.925.875
C18.452.584.500.937
C18.452.648.398.850
C18.452.648.925.875
Definição Inglês:   An autosomal recessive disorder of CHOLESTEROL metabolism. It is caused by a deficiency of 7-dehydrocholesterol reductase, the enzyme that converts 7-dehydrocholesterol to cholesterol, leading to an abnormally low plasma cholesterol. This syndrome is characterized by multiple CONGENITAL ABNORMALITIES, growth deficiency, and INTELLECTUAL DISABILITY. 
Nota Histórica Inglês:   1996 
Qualificadores Permitidos Inglês:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
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  
Número do Registro:   32609 
Identificador Único:   D019082 

Ocorrência na BVS:
 

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