Literature DB >> 1015980

[Hereditary fructose intolerance with early onset].

J C Mercier, A Bourrillon, F Beaufils, M Odievre.   

Abstract

Four cases of hereditary fructose intolerance with an early onset are reported. The features of acute liver failure in the neonatal period include a haemorrhagic syndrome, collapse, neurological features, hypoglycaemia, disturbed bleeding and clotting studies and abnormal liver function tests. Investigations into the aetiology include a search for bacterial or viral infection but particularly for a metabolic cause: especially for hereditary fructose intolerance which may be difficult to distinguish from tyrosinosis. Finally, methods of treatment are discussed: continuous glucose infusion, exchange transfusion, assisted ventilation, and dietary measures beginning with protein exclusion. The importance of careful observation is stressed (particularly sequential studies of bloodclotting factors).

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Year:  1976        PMID: 1015980

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN: 0003-9764


  1 in total

1.  Haemorrhagic diathesis as a possible early sign of hereditary fructose intolerance.

Authors:  A Hosková; A Mrskos
Journal:  Eur J Pediatr       Date:  1977-12-30       Impact factor: 3.183

  1 in total

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