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Descritor em português: Síndrome de Laron
Descritor em inglês: Laron Syndrome
Descritor em espanhol: Síndrome de Laron
Descritor síndrome de Laron
Termo(s) alternativo(s) síndrome de insensibilidad a la hormona del crecimiento
Nota de escopo: Trastorno autosómico recesivo caracterizado por estatura baja, alteración del RECEPTOR DE HORMONA DEL CRECIMIENTO e imposibilidad para producir el FACTOR I DEL CRECIMIENTO SIMILAR A LA INSULINA por la acción de la HORMONA DEL CRECIMIENTO. El síndrome de Laron no es una forma de enanismo hipofisario primario (ENANISMO POR DEFICIENCIA DE HORMONA DEL CRECIMIENTO) sino el resultado de la mutación del gen humano GHR en el cromosoma 5.
Descritor em francês: Syndrome de Laron
Termo(s) alternativo(s): Dwarfism II, Pituitary
Dwarfism IIs, Pituitary
Dwarfism, Laron
GH Resistance, Primary
Growth Hormone Insensitivity Syndrome
Growth Hormone Receptor Defect
Growth Hormone Receptor Deficiency
Laron Dwarfism
Laron Type Dwarfism I
Pituitary Dwarfism II
Pituitary Dwarfism IIs
Primary GH Resistance
Primary Growth Hormone Resistance
Severe GH Insensitivity
Syndrome, Laron
Código(s) hierárquico(s): C05.116.099.343.679
C16.320.240.750
C19.297.656
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D046150
Nota de escopo: An autosomal recessive disorder characterized by short stature, defective GROWTH HORMONE RECEPTOR, and failure to generate INSULIN-LIKE GROWTH FACTOR I by GROWTH HORMONE. Laron syndrome is not a form of primary pituitary dwarfism (GROWTH HORMONE DEFICIENCY DWARFISM) but the result of mutation of the human GHR gene on chromosome 5.
Qualificadores permitidos: 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
Indexação Anterior: Dwarfism (1976-2004)
Growth Hormone (1976-2004)
Receptors, Cell Surface (1976-2004)
Receptors, Somatotropin (1991-2004)
Nota MeSH pública: 2005
Nota histórica: 2005
Identificador DeCS: 38609
ID do descritor: D046150
Classificação da NLM: WK 550
Documentos indexados na Biblioteca Virtual em Saúde (BVS): Clique aqui para acessar os documentos da BVS
Data de estabelecimento: 01/01/2005
Data de entrada: 07/07/2004
Data de revisão: 03/07/2012
Laron Syndrome - Conceito preferido
Identificador do conceito M0452907
Nota de escopo An autosomal recessive disorder characterized by short stature, defective GROWTH HORMONE RECEPTOR, and failure to generate INSULIN-LIKE GROWTH FACTOR I by GROWTH HORMONE. Laron syndrome is not a form of primary pituitary dwarfism (GROWTH HORMONE DEFICIENCY DWARFISM) but the result of mutation of the human GHR gene on chromosome 5.
Termo preferido Laron Syndrome
Termo(s) alternativo(s) Dwarfism II, Pituitary
Dwarfism IIs, Pituitary
Dwarfism, Laron
GH Resistance, Primary
Growth Hormone Insensitivity Syndrome
Growth Hormone Receptor Defect
Growth Hormone Receptor Deficiency
Laron Dwarfism
Laron Type Dwarfism I
Pituitary Dwarfism II
Pituitary Dwarfism IIs
Primary GH Resistance
Primary Growth Hormone Resistance
Severe GH Insensitivity
Syndrome, Laron



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