Literature DB >> 7017570

Metabolic abnormalities in the idiopathic Fanconi syndrome: studies of carbohydrate metabolism in two patients.

R W Chesney, B S Kaplan, D Teitel, E Colle, R R McInnes, H Goldman, C R Scriver.   

Abstract

Two patients with idiopathic Fanconi syndrome and glucose intolerance were studied from a metabolic perspective. They had fasting hyperglycemia, massive glucosuria, insulinopenia, ketosis, and elevated serum free fatty acids. There was a markedly blunted insulin secretory response to glucagon, tolbutamide, glucose, and arginine. One patient had the findings of diabetic retinopathy and a sensory neuropathy. Neither patient could convert galactose to glucose, but they did not have galactosemia. As a result of these studies, and previous reports in which similar changes were noted, we conclude that diabetes mellitus may occur in patients who have had idiopathic Fanconi syndrome for many years.

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Year:  1981        PMID: 7017570

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  3 in total

1.  Glycogen storage disease, Fanconi nephropathy, abnormal galactose metabolism and mitochondrial myopathy.

Authors:  H Hurvitz; O N Elpeleg; V Barash; E Kerem; R M Reifen; W Ruitenbeek; C Mor; D Branski
Journal:  Eur J Pediatr       Date:  1989-10       Impact factor: 3.183

2.  Fanconi-Bickel syndrome.

Authors:  F Manz; H Bickel; J Brodehl; D Feist; K Gellissen; B Geschöll-Bauer; G Gilli; E Harms; H Helwig; W Nützenadel
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

3.  Diabetes-like renal glomerular disease in Fanconi-Bickel syndrome.

Authors:  G T Berry; L Baker; F S Kaplan; C L Witzleben
Journal:  Pediatr Nephrol       Date:  1995-06       Impact factor: 3.714

  3 in total

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