[Study of glucagon secretion in patients with hemochromatosis]. 1977

J J Gonvers, and L Henchoz, and J R Hofstetter, and W A Muller

Diabetes in idiopathic hemochromatosis has been considered to be secondary to islet cell damage resulting from the iron deposits. Plasma glucagon was measured by immunoassay using the pancreas specific 30-K antiserum, and was found to be normal or slightly elevated during arginine-infusion tests in patients exhibiting both hemochromatosis and pathological glucose tolerance. This suggests that diabetes in hemochromatosis is not due to a lesion resulting from the iron deposits. The two affections appear to be merely associated and are possibly genetically linked.

UI MeSH Term Description Entries
D003920 Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE.
D005934 Glucagon A 29-amino acid pancreatic peptide derived from proglucagon which is also the precursor of intestinal GLUCAGON-LIKE PEPTIDES. Glucagon is secreted by PANCREATIC ALPHA CELLS and plays an important role in regulation of BLOOD GLUCOSE concentration, ketone metabolism, and several other biochemical and physiological processes. (From Gilman et al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 9th ed, p1511) Glucagon (1-29),Glukagon,HG-Factor,Hyperglycemic-Glycogenolytic Factor,Proglucagon (33-61),HG Factor,Hyperglycemic Glycogenolytic Factor
D006432 Hemochromatosis A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) Diabetes, Bronze,Bronze Diabetes,Bronzed Cirrhosis,Familial Hemochromatosis,Genetic Hemochromatosis,Haemochromatosis,Hemochromatoses,Iron Storage Disorder,Pigmentary Cirrhosis,Primary Hemochromatosis,Troisier-Hanot-Chauffard Syndrome,Von Recklenhausen-Applebaum Disease,Bronzed Cirrhoses,Cirrhoses, Bronzed,Cirrhoses, Pigmentary,Cirrhosis, Bronzed,Cirrhosis, Pigmentary,Disease, Von Recklenhausen-Applebaum,Diseases, Von Recklenhausen-Applebaum,Disorder, Iron Storage,Disorders, Iron Storage,Familial Hemochromatoses,Genetic Hemochromatoses,Haemochromatoses,Hemochromatose,Hemochromatoses, Familial,Hemochromatoses, Genetic,Hemochromatosis, Familial,Hemochromatosis, Genetic,Iron Storage Disorders,Pigmentary Cirrhoses,Recklenhausen-Applebaum Disease, Von,Recklenhausen-Applebaum Diseases, Von,Storage Disorder, Iron,Storage Disorders, Iron,Syndrome, Troisier-Hanot-Chauffard,Syndromes, Troisier-Hanot-Chauffard,Troisier Hanot Chauffard Syndrome,Troisier-Hanot-Chauffard Syndromes,Von Recklenhausen Applebaum Disease,Von Recklenhausen-Applebaum Diseases
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

J J Gonvers, and L Henchoz, and J R Hofstetter, and W A Muller
May 1978, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme,
J J Gonvers, and L Henchoz, and J R Hofstetter, and W A Muller
September 1977, Diabetologia,
J J Gonvers, and L Henchoz, and J R Hofstetter, and W A Muller
February 1982, The Journal of clinical endocrinology and metabolism,
J J Gonvers, and L Henchoz, and J R Hofstetter, and W A Muller
June 1974, Diabetes,
J J Gonvers, and L Henchoz, and J R Hofstetter, and W A Muller
July 1973, Horumon to rinsho. Clinical endocrinology,
J J Gonvers, and L Henchoz, and J R Hofstetter, and W A Muller
March 2019, Endocrine,
J J Gonvers, and L Henchoz, and J R Hofstetter, and W A Muller
April 2016, Journal of diabetes and its complications,
J J Gonvers, and L Henchoz, and J R Hofstetter, and W A Muller
April 2016, Journal of hepatology,
J J Gonvers, and L Henchoz, and J R Hofstetter, and W A Muller
April 1972, Helvetica medica acta,
J J Gonvers, and L Henchoz, and J R Hofstetter, and W A Muller
August 1969, The British journal of surgery,
Copied contents to your clipboard!