Galactosaemia: Early treatment with an elemental formula

Journal of Inherited Metabolic Disease

Volumn 28, Issue 2, 2005, Pages 163-168

  Zlatunich, C O ^a   Packman, S ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GALACTITOL; GALACTOSE 1 PHOSPHATE URIDYLYLTRANSFERASE;

ARTICLE; ARTIFICIAL MILK; CASE REPORT; CORRELATION FUNCTION; DIET THERAPY; ELEMENTAL DIET; FEMALE; GALACTOSEMIA; HUMAN; HYPERBILIRUBINEMIA; INFANT FEEDING; NEWBORN; PHOTOTHERAPY; PROGNOSIS; URINE LEVEL;

ERYTHROCYTES; FEMALE; FOOD, FORMULATED; GALACTOSE; GALACTOSEMIAS; GALACTOSEPHOSPHATES; HUMANS; INFANT FORMULA; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES;

EID: 19444385243     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10545-005-5516-2     Document Type: Article

References (20)

1. Acosta PB, Gross KC (1995) Hidden sources of galactose in the environment. Eur J Pediatr 154(1): 1-6.
2. De Boissieu D, Matarazzo P, Dupont C (1997) Allergy to extensively hydrolyzed cow milk proteins in infants: Identification and treatment with an amino acid-based formula. J Pediatr 131(5): 744-747.
3. Gitzelmann R, Hanson RG (1974) Galactose biogenesis and disposal in galactosemics. Biochem Biophys Acta 372: 374-378.
4. Gropper SS, Gross KC, Olds SJ (1993) Galactose content of selected fruit and vegetable baby foods: Implications for infants on galactose-restricted diets. J Am Diet Assoc 93: 328-330.
5. Gropper SS, Weese JO, West PA, et al (2000) Free galactose content of fresh fruits and vegetable baby foods. J Am Diet Assoc 100(5): 573-575.
6. Gross KC, Acosta PB (1991) Fruits and vegetables are a source of galactose: Implications in planning the diets of patients with galactosaemia. J Inherit Metab Dis 14: 253-258.
7. Hill DJ, Heine RG, Cameron DJS, et al (1999) The natural history of intolerance to soy and extensively hydrolyzed formula in infants with multiple food protein intolerance. J Pediatr 135(1): 118-121.
8. Holton J, Walter J, Tyfield L (2001) Galactosemia. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds; Childs B, Kinzler KW, Vogelstein B, assoc. eds. The Metabolic and Molecular Bases of Inherited Disease, 8th edn. New York: McGraw-Hill, 1561-1575.
9. Hutchesson AC, Murdoch-Davis C, Green A, et al (1999) Biochemical monitoring of treatment for galactosaemia: Biological variability in metabolite concentrations. J Inherit Metab Dis 22: 139-148.
10. Irons M, Levy HL, Reuschel S (1985) The accumulation of galactose-1-phosphate in the galactosemic fetus despite milk avoidance. J Pediatr 107: 261-263.
11. Isolauri E, Yelda S, Makinen-Kiljunen S, et al (1995) Efficacy and safety of hydrolyzed cow milk and amino acid-derived formulas in infants with cow milk allergy. J Pediatr 127(4): 550-557.
12. Jakobs C, Schweitzer S, Dorland B (1995) Galactitol in galactosemia. Eur J Pediatr 154 (supplement 2): S50-S52.
13. Ng W, Donnell G, Bergren W, et al (1977) Prenatal diagnosis of galactosemia. Clin Chim Acta 74: 227.
14. 13C) galactose isotope enrichment. Mol Genet Metab 70: 261-271.
15. Palmieri M, Mazur A, Berry GT, et al (1999) Urine and plasma galactitol in patients with galactose-1-phosphate uridyltransferase deficiency galactosemia. Metabolism 48: 1294-1302.
16. Ross Laboratories (2001) Protocol 14 - Galactosemia: Nutrition Support of Infants, Children, and Adults with Isomil ® Soy Formula with Iron. Nutrition Support Protocols - 4th Edition 262-278.
17. Schadewaldt P, Killius S, Kamalanathan L, et al (2003) Renal excretion of galactose and galactitol in patients with classical galactosaemia, obligate heterozygous parents and healthy subjects. J Inherit Metab Dis 26: 459-479.
18. Schweitzer S, Shin Y, Jakobs C, et al (1993) Long-term outcome in 134 patients with galactosaemia. Eur J Pediatr 152: 36-43.
19. Tyfield L, Stephenson A, Holton JB (1997) Mutation analysis and psychometric assessments in the galactosaemic population of the British Isles. J Med Genet 34: S18.
20. Waggoner D, Buist N, Donnell G (1990) Long-term prognosis in galactosaemia: Results of a survey of 350 cases. J Inherit Metab Dis 13: 802-818.