Nesidioblastosis
"Nesidioblastosis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
Descriptor ID |
D046768
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MeSH Number(s) |
C06.689.150.500 C16.614.200.500 C18.452.394.968.250.500 C18.452.394.984.200.500
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Concept/Terms |
Nesidioblastosis- Nesidioblastosis
- Nesidioblastoses
- Pancreatic Nesidioblastosis
- Nesidioblastoses, Pancreatic
- Nesidioblastosis, Pancreatic
- Pancreatic Nesidioblastoses
- Hyperinsulinism, Familial, with Pancreatic Nesidioblastosis
- Nesidioblastosis of Pancreas
- Pancreas Nesidioblastoses
- Pancreas Nesidioblastosis
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Below are MeSH descriptors whose meaning is more general than "Nesidioblastosis".
Below are MeSH descriptors whose meaning is more specific than "Nesidioblastosis".
This graph shows the total number of publications written about "Nesidioblastosis" by people in UAMS Profiles by year, and whether "Nesidioblastosis" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Nesidioblastosis" by people in Profiles over the past ten years.
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Orujov M, Lai KK, Forse CL. Concurrent Adult-Onset Diffuse ?-Cell Nesidioblastosis and Pancreatic Neuroendocrine Tumor: A Case Report and Review of the Literature. Int J Surg Pathol. 2019 Dec; 27(8):912-918.