Literature DB >> 76370

[Postoperative fructose infusion in a case of presumed hereditary fructose intolerance (author's transl)].

J M Hackl, D Balogh, F Kunz, E Dworzak, B Puschendorf, A Decristoforo, F Maier.   

Abstract

Hereditary fructose intolerance (HFI) was diagnosed in a 61 year-old male patient on account of liver dysfunction followed by prolonged shock immediately after the administration of a fructose and lactose infusion postoperatively. The diagnosis of HFI was based on an increased value of fructose, hypoglycaemia, lactic acidosis and diminution of the phosphate level in combination with the typical family history. The patient's children showed a normal reaction to fructose administration. The therapy included glucose, insulin and heparin administration, balance of acidosis and partial exchange of blood, which resulted in improvement in the glucose level, coagulation factors and acidosis, but could not prevent further liver damage and uraemia with a fatal outcome.

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Year:  1978        PMID: 76370

Source DB:  PubMed          Journal:  Wien Klin Wochenschr        ISSN: 0043-5325            Impact factor:   1.704


  4 in total

1.  Iatrogenic deaths in hereditary fructose intolerance.

Authors:  T M Cox
Journal:  Arch Dis Child       Date:  1993-10       Impact factor: 3.791

Review 2.  [Repeated perioperative administration of fructose and sorbitol in a female patient with hereditary fructose intolerance [HFI)].

Authors:  M Sachs; F Asskali; H Förster; A Encke
Journal:  Z Ernahrungswiss       Date:  1993-03

Review 3.  Hereditary fructose intolerance.

Authors:  M Ali; P Rellos; T M Cox
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

4.  Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population.

Authors:  Erin M Coffee; Laura Yerkes; Elizabeth P Ewen; Tiffany Zee; Dean R Tolan
Journal:  J Inherit Metab Dis       Date:  2009-12-23       Impact factor: 4.982

  4 in total

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