Intravenous glycerol therapy should not be used in patients with unrecognized fructose-1,6-bisphosphatase deficiency

Author:

HASEGAWA YUKIHIRO,KIKAWA YOSHIHARU,MIYAMAOTO JUNKO,SUGIMOTO SHUJI,ADACHI MASANORI,OHURA TOSHIHIRO,MAYUMI MITSUFUMI

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health

Reference15 articles.

1. FASTING HYPOGLYCÆMIA AND METABOLIC ACIDOSIS ASSOCIATED WITH DEFICIENCY OF HEPATIC FRUCTOSE-1,6-DIPHOSPHATASE ACTIVITY

2. INVESTIGATION OF INBORN ERRORS OF METABOLISM IN UNEXPECTED INFANT DEATHS

3. 3 B Steinmann, R Gitzelmann, and G. van den Berghe Essential fructosuria hereditary fructose intolerance, and fructose-l,6-diphosphatase deficiency. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds).The Metabolic Basis of Inherited Disease. McGraw Hill, New York, 2001; 1489-520.

4. 4 BK. Burton Inherited metabolic disorders. In: Avery GB, Fletcher MA, MacDonald MG (eds).Neonatology: Pathophysiology and Management of the Newborn. Lippincott Williams & Wilkins, Philadelphia, 1999; 821-37.

5. 5 A Hill, and JJ. Volpe Neurological and neuromuscular disorders. In: Avery GB, Fletcher MA, MacDonald MG (eds).Neonatology; Pathophysiology and Management of the Newborn. Lippincott Williams & Wilkins, Philadelphia, 1999; 1231-52.

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