Number of the records: 1

nezidioblastóza

Subject h.	nezidioblastóza
Subject h.	Nesidioblastosis
Entry terms	hyperinzulinizmus familiárny, s nezidioblastózou pankreasu
English X references	Hyperinsulinism, Familial, with Pancreatic Nesidioblastosis
Scope note in English	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.
See also reference (FX) in Slovak	ATP-viažuce kazetové transportéry KATP kanály
See also reference (FX) in English	ATP-Binding Cassette Transporters KATP Channels
Links	(1) - ARTICLES
	(2) - MeSH descriptor

subject heading

Number of the records: 1