Pesquisa
Descritor em português: Hiperinsulinismo Congênito
Descritor em inglês: Congenital Hyperinsulinism
Descritor em espanhol: Hiperinsulinismo Congénito
Descritor hiperinsulinismo congénito
Termo(s) alternativo(s) hipoglucemia con hiperinsulinemia persistente del lactante
hipoglucemia hiperinsulinémica persistente de la infancia
hipoglucemia hiperinsulinémica persistente del lactante
Nota de escopo: HIPOGLUCEMIA familiar no transitoria, con defectos en la retroalimentación negativa de liberación de INSULINA regulada por GLUCOSA. Entre los fenotipos clínicos se incluyen: HIPOGLUCEMIA, HIPERINSULINEMIA, CRISIS CONVULSIVAS, COMA y, a menudo, gran PESO AL NACER. Existen diversos subtipos, el más común el tipo 1, que se asocia a mutaciones en los TRANSPORTADORES DE CASETE DE UNIÓN A ATP (subfamilia C, miembro 8).
Descritor em francês: Hyperinsulinisme congénital
Termo(s) alternativo(s): Congenital Hyperinsulinisms
Familial Hyperinsulinemic Hypoglycemia 1
Familial Hyperinsulinism
Familial Hyperinsulinisms
Hyperinsulinemia Hypoglycemia of Infancy
Hyperinsulinemic Hypoglycemia Due to Focal Adenomatous Hyperplasia
Hyperinsulinemic Hypoglycemia, Familial, 1
Hyperinsulinemic Hypoglycemia, Familial, 2
Hyperinsulinemic Hypoglycemia, Persistent
Hyperinsulinemic Hypoglycemias, Persistent
Hyperinsulinism, Congenital
Hyperinsulinism, Familial
Hyperinsulinism, Neonatal
Hyperinsulinisms, Congenital
Hyperinsulinisms, Familial
Hyperinsulinisms, Neonatal
Hypoglycemia, Hyperinsulinemic, of Infancy
Hypoglycemia, PHHI
Hypoglycemia, Persistent Hyperinsulinemic
Hypoglycemias, PHHI
Hypoglycemias, Persistent Hyperinsulinemic
Infancy Hyperinsulinemia Hypoglycemia
Infancy Hyperinsulinemia Hypoglycemias
Neonatal Hyperinsulinism
Neonatal Hyperinsulinisms
PHHI Hypoglycemia
PHHI Hypoglycemias
Persistent Hyperinsulinemia Hypoglycemia of Infancy
Persistent Hyperinsulinemic Hypoglycemia
Persistent Hyperinsulinemic Hypoglycemias
Código(s) hierárquico(s): C06.689.150
C16.614.200
C18.452.394.968.250
C18.452.394.984.200
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D044903
Nota de escopo: A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMIA; HYPERINSULINEMIA; SEIZURES; COMA; and often large BIRTH WEIGHT. Several sub-types exist with the most common, type 1, associated with mutations on an ATP-BINDING CASSETTE TRANSPORTERS (subfamily C, member 8).
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: Chromosomes, Human, Pair 11 (1995-2003)
Hyperinsulinism (1977-2003)
Hypoglycemia (1977-2003)
Nota MeSH pública: 2014; see PERSISTENT HYPERINSULINEMIA HYPOGLYCEMIA OF INFANCY 2004-2013
Nota histórica: 2014(2004)
Veja também os descritores: ATP-Binding Cassette Transporters MeSH
Potassium Channels, Inwardly Rectifying MeSH
Identificador DeCS: 38055
ID do descritor: D044903
Documentos indexados na Biblioteca Virtual em Saúde (BVS): Clique aqui para acessar os documentos da BVS
Data de estabelecimento: 01/01/2004
Data de entrada: 09/07/2003
Data de revisão: 08/07/2013
Congenital Hyperinsulinism - Conceito preferido
Identificador do conceito M0446507
Nota de escopo A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMIA; HYPERINSULINEMIA; SEIZURES; COMA; and often large BIRTH WEIGHT. Several sub-types exist with the most common, type 1, associated with mutations on an ATP-BINDING CASSETTE TRANSPORTERS (subfamily C, member 8).
Termo preferido Congenital Hyperinsulinism
Termo(s) alternativo(s) Congenital Hyperinsulinisms
Familial Hyperinsulinism
Familial Hyperinsulinisms
Hyperinsulinemia Hypoglycemia of Infancy
Hyperinsulinemic Hypoglycemia, Persistent
Hyperinsulinemic Hypoglycemias, Persistent
Hyperinsulinism, Congenital
Hyperinsulinism, Familial
Hyperinsulinism, Neonatal
Hyperinsulinisms, Congenital
Hyperinsulinisms, Familial
Hyperinsulinisms, Neonatal
Hypoglycemia, Hyperinsulinemic, of Infancy
Hypoglycemia, PHHI
Hypoglycemia, Persistent Hyperinsulinemic
Hypoglycemias, PHHI
Hypoglycemias, Persistent Hyperinsulinemic
Infancy Hyperinsulinemia Hypoglycemia
Infancy Hyperinsulinemia Hypoglycemias
Neonatal Hyperinsulinism
Neonatal Hyperinsulinisms
PHHI Hypoglycemia
PHHI Hypoglycemias
Persistent Hyperinsulinemia Hypoglycemia of Infancy
Persistent Hyperinsulinemic Hypoglycemia
Persistent Hyperinsulinemic Hypoglycemias
Hyperinsulinemic Hypoglycemia, Familial, 2 - Mais específico
Identificador do conceito M0532834
Termo preferido Hyperinsulinemic Hypoglycemia, Familial, 2
Familial Hyperinsulinemic Hypoglycemia 1 - Mais específico
Identificador do conceito M0570812
Termo preferido Familial Hyperinsulinemic Hypoglycemia 1
Termo(s) alternativo(s) Hyperinsulinemic Hypoglycemia Due to Focal Adenomatous Hyperplasia
Hyperinsulinemic Hypoglycemia, Familial, 1



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