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Concept information

Digestive System Diseases > Pancreatic Diseases > Congenital Hyperinsulinism > Nesidioblastosis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Congenital Hyperinsulinism > Nesidioblastosis
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Glucose Metabolism Disorders > Hyperinsulinism > Congenital Hyperinsulinism > Nesidioblastosis
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Glucose Metabolism Disorders > Hypoglycemia > Congenital Hyperinsulinism > Nesidioblastosis

Terme préférentiel

Nesidioblastosis  

Type

  • mesh:Descriptor

Définition

  • An inherited autosomal recessive syndrome characterized by the disorganized formation of new islets in the PANCREAS and CONGENITAL HYPERINSULINISM. It is due to focal hyperplasia of pancreatic ISLET CELLS budding off from the ductal structures and forming new islets of Langerhans. Mutations in the islet cells involve the potassium channel gene KCNJ11 or the ATP-binding cassette transporter gene ABCC8, both on CHROMOSOME 11.

Concept générique

Concepts associés

Synonyme(s)

  • Hyperinsulinism, Familial, with Pancreatic Nesidioblastosis
  • Nesidioblastosis of Pancreas
  • Pancreatic Nesidioblastosis

Qualificatif(s) autorisé(s)

Traductions

  • Nésidioblastose

    français

  • Hyperinsulinisme diffus
  • Nésidioblastose du pancréas
  • Nésidioblastose pancréatique

URI

http://data.loterre.fr/ark:/67375/JVR-QB0SMP7M-N

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RDF/XML TURTLE JSON-LD Date de création 07/07/2004, dernière modification le 03/07/2012