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تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
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Causes of hypoglycemia in infants and children

Causes of hypoglycemia in infants and children
Disorder MIM # Typical age group
Insulin-mediated
Hyperinsulinism
Congenital   Neonatal, infancy
KATP hyperinsulinism 256450,
601820
 
GLUD1 hyperinsulinism 606762  
GCK hyperinsulinism 602485  
Perinatal stress-induced hyperinsulinism   Neonatal
Syndromic hyperinsulinism    
Beckwith-Wiedemann syndrome 130650 Neonatal, infancy
Kabuki syndrome 147920 Neonatal, infancy
Insulinoma
Associated with MEN1 131100 Adolescence
Factitious hypoglycemia   Any age
Congenital disorders of glycosylation
Phosphomannomutase 2 deficiency 212065 Infancy, childhood
Phosphoglucomutase 1 deficiency 614921 Any age
Mannosephosphate isomerase deficiency 602579 Infancy
Fatty acid oxidation disorders
Medium-chain acyl-CoA dehydrogenase 201450 Infancy
20+ other disorders   All ages
Ketotic hypoglycemia
Disorders of glycogen metabolism
Glycogen storage disease type 0 240600 Early childhood
Glycogen storage disease type III 232400 Infancy
Glycogen storage disease type VI 232700 Early childhood
Glycogen storage disease type IX 306000 Early childhood
Hormone deficiencies
Growth hormone deficiency   Infancy, early childhood
Cortisol deficiency   Childhood
Ketone utilization defects 245050,
203750,
616095
Early childhood
Idiopathic ketotic hypoglycemia   Early childhood
Disorders of gluconeogenesis
Glycogen storage type I* 232200 Infancy
Fructose-1,6-bisphosphatase deficiency 229700 Infancy, early childhood
Pyruvate carboxylase deficiency 266150 Infancy
PEPCK deficiency 261650 Infancy
Galactosemia 230400;
others
Infancy
Hereditary fructose intolerance 229600 Infancy, childhood
Other causes
Ingestions   Early childhood, all ages
Oral hypoglycemic    
Ethanol   Adolescence
Salicylates    
Beta blockers    
Pentamidine    
6-mercaptopurine    
Ackee/lychee fruit    
Liver failure   All ages
Sepsis   Infancy, childhood
MIM: Mendelian Inheritance in Man database; KATP: ATP-sensitive potassium channel; GLUD1: glutamate dehydrogenase 1 gene; GCK: glucokinase gene; MEN1: multiple endocrine neoplasia type 1; PEPCK: phosphoenolpyruvate carboxykinase.
* Also, disorders of glycogen metabolism.
Graphic 103015 Version 7.0

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