Structured Summary
Abstract
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.
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Synonyms
9 entry terms
- Hyperinsulinism, Familial, with Pancreatic Nesidioblastosis
- Nesidioblastosis of Pancreas
- Pancreatic Nesidioblastosis
- Nesidioblastoses
- Nesidioblastoses, Pancreatic
- Nesidioblastosis, Pancreatic
- Pancreas Nesidioblastoses
- Pancreas Nesidioblastosis
- Pancreatic Nesidioblastoses
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
2005; use PANCREATIC DISEASES 1983-2004
MeSH Record
Previous Indexing
- Hyperinsulinism (1971-2004)
- Hyperplasia (1968-2004)
- Islets of Langerhans (1968-2004)
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AMA Style
References
- National Library of Medicine. Nesidioblastosis. Medical Subject Headings (MeSH). 2026. Unique ID D046768. http://id.nlm.nih.gov/mesh/2026/D046768
- Nesidioblastosis. In: Wikipedia. https://en.wikipedia.org/wiki/Nesidioblastosis
- Nesidioblastosis. In: Wikidata. https://www.wikidata.org/wiki/Q1535394