Expresión de búsqueda: PERSISTENT HYPERINSULINEMIA HYPOGLYCEMIA OF INFANCY 
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Descriptor Inglés:   Persistent Hyperinsulinemia Hypoglycemia of Infancy 
Descriptor Español:   Hipoglicemia Hiperinsulinémica Persistente del Lactante 
Descriptor Portugués:   Hipoglicemia Hiperinsulinęmica Persistente do Lactente 
Categoría:   C16.614.716
C18.452.394.968.750
C18.452.394.984.746
Definición Inglés:   A form of nontransient HYPOGLYCEMIA, unique to infancy, due to autosomal recessive mutations of the sulfonylurea receptor gene on CHROMOSOME 11. Defects in the sulfonylurea receptors (ATP-BINDING CASSETTE TRANSPORTERS) on the PANCREATIC BETA CELLS prevent negative feedback of GLUCOSE-regulated INSULIN release thus resulting in HYPERINSULINEMIA. Clinical phenotype includes SEIZURES; COMA; and often large BIRTH WEIGHT for GESTATIONAL AGE. 
Nota Histórica Inglés:   2004 
Calificadores Permitidos Inglés:  
blood cerebrospinal fluid
chemically induced classification
complications diet therapy
diagnosis drug therapy
economics ethnology
embryology enzymology
epidemiology etiology
genetics history
immunology metabolism
microbiology mortality
nursing pathology
prevention & control physiopathology
parasitology psychology
radiography rehabilitation
radionuclide imaging radiotherapy
surgery therapy
urine ultrasonography
veterinary virology
Número del Registro:   38055 
Identificador Único:   D044903 

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