نتایج جستجو برای: hyperinsulinism

تعداد نتایج: 5435  

Journal: :Journal of molecular endocrinology 2015
Sofia A Rahman Azizun Nessa Khalid Hussain

Congenital hyperinsulinism (CHI) is a complex heterogeneous condition in which insulin secretion from pancreatic β-cells is unregulated and inappropriate for the level of blood glucose. The inappropriate insulin secretion drives glucose into the insulin-sensitive tissues, such as the muscle, liver and adipose tissue, leading to severe hyperinsulinaemic hypoglycaemia (HH). At a molecular level, ...

Journal: :Hormone research 2006
Irina Giurgea Christine Bellanné-Chantelot Maria Ribeiro Laurence Hubert Christine Sempoux Jean-Jacques Robert Oliver Blankenstein Kahlid Hussain Francis Brunelle Claire Nihoul-Fékété Jacques Rahier Francis Jaubert Pascale de Lonlay

Congenital hyperinsulinism (CHI), characterized by profound hypoglycaemia related to inappropriate insulin secretion, may be associated histologically with either diffuse insulin hypersecretion or focal adenomatous hyperplasia, which share a similar clinical presentation, but result from different molecular mechanisms. Whereas diffuse CHI is of autosomal recessive, or less frequently of autosom...

2013
Adam Stevens Karen E Cosgrove Raja Padidela Mars S Skae Peter E Clayton Indraneel Banerjee Mark J Dunne

Congenital Hyperinsulinism is a condition with a number of genetic causes, but for the majority of patients, the underlying aetiology is unknown. We present here a rational argument for the use of computational biology as a valuable resource for identifying new candidate genes which may cause disease and for understanding the complex mechanisms which define the pathophysiology of this rare dise...

Journal: :Archives of disease in childhood 2003
S Srinivasan M J Waters J E Rowland R C Baxter C F Verge

We report a 5 year old girl with postnatal overgrowth (height velocity >97th centile), hyperinsulinaemia, and increased insulin-like growth factor 1 for age, without evidence of bioactive or immunoreactive growth hormone excess or pituitary abnormality. Although her overgrowth may be a result of hyperinsulinism, her serum contains a factor (neither insulin nor IGF-1) which is able to stimulate ...

2016

Congenital hyperinsulinism (HI) is the most common cause of persistent hypoglycemia in infants and children. In cases of diazoxide-unresponsive HI, alternative medical and surgical approaches may be required to reduce the risk of hypoglycemia. Octreotide, a somatostatin analog, often has a role Received: December 18, 2015 Accepted: January 12, 2016 Published online: February 12, 2016 HORMONE

Journal: :Journal of Clinical Research in Pediatric Endocrinology 2018

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