Ha seleccionado la visión en Inglés
Descriptor en español: |
Nesidioblastosis
| ||||||
Descriptor en inglés: | Nesidioblastosis | ||||||
Descriptor en portugués: | Nesidioblastose | ||||||
Descriptor en francés: | Nésidioblastose | ||||||
Término(s) alternativo(s): |
Hyperinsulinism, Familial, with Pancreatic Nesidioblastosis Nesidioblastoses Nesidioblastoses, Pancreatic Nesidioblastosis of Pancreas Nesidioblastosis, Pancreatic Pancreas Nesidioblastoses Pancreas Nesidioblastosis Pancreatic Nesidioblastoses Pancreatic Nesidioblastosis |
||||||
Código(s) jeráquico(s): |
C06.689.150.500 C16.614.200.500 C18.452.394.968.250.500 C18.452.394.984.200.500 |
||||||
Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D046768 | ||||||
Nota de alcance: | 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. |
||||||
Calificadores 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 |
||||||
Indexación anterior: |
Hyperinsulinism (1971-2004) Hyperplasia (1968-2004) Islets of Langerhans (1968-2004) |
||||||
Nota Pública de MeSH: | 2005; see PANCREATIC DISEASES 1983-2004 |
||||||
Nota de historia: | 2005; use PANCREATIC DISEASES 1983-2004 |
||||||
Vea también los descriptores: |
ATP-Binding Cassette Transporters
MeSH KATP Channels MeSH | ||||||
Identificador de DeCS: | 38627 | ||||||
ID del Descriptor: | D046768 | ||||||
Documentos indizados en la Biblioteca Virtual de Salud (BVS): | Haga clic aquí para acceder a los documentos de la BVS | ||||||
Fecha de establecimiento: | 01/01/2005 | ||||||
Fecha de entrada: | 07/07/2004 | ||||||
Fecha de revisión: | 03/07/2012 |
|
Nesidioblastosis
- Concepto preferido
UI del concepto |
M0015793 |
Nota de alcance | 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. |
Término preferido | Nesidioblastosis |
Término(s) alternativo(s) |
Hyperinsulinism, Familial, with Pancreatic Nesidioblastosis Nesidioblastoses Nesidioblastoses, Pancreatic Nesidioblastosis of Pancreas Nesidioblastosis, Pancreatic Pancreas Nesidioblastoses Pancreas Nesidioblastosis Pancreatic Nesidioblastoses Pancreatic Nesidioblastosis |
Queremos sus comentarios sobre el nuevo sitio web de DeCS / MeSH
Lo invitamos a completar una encuesta que no tomará más de 3 minutos.
Ir a la encuesta