Nutrition in metabolic disease

Paediatrics and Child Health

Volumn 21, Issue 9, 2011, Pages 401-405

  Jameson, Elisabeth ^a   Morris, Andrew A M ^a  

^a ST MARY S HOSPITAL   (United Kingdom)

Author keywords

Catabolism; Emergency regimen; Encephalopathy; Inborn errors of metabolism; Ketogenic diet; Low protein diet; Protein exchange; Protein supplements

Indexed keywords

CALOREEN; GALACTOSE; GLUCOSE; GLUCOSE POLYMER; GLUCOSE TRANSPORTER 1; MAXIJUL; PHENYLALANINE; POLYCAL; UNCLASSIFIED DRUG; VITAJOULE;

ABETALIPOPROTEINEMIA; ACUTE BRAIN DISEASE; AMINO ACID DEFICIENCY; CATABOLISM; CHILD NUTRITION; DIET RESTRICTION; DIETARY INTAKE; ENERGY METABOLISM; ENTERIC FEEDING; FAMILIAL HYPERCHOLESTEROLEMIA; FATTY ACID OMEGA OXIDATION; GALACTOSEMIA; GASTROSTOMY; GLYCOGEN STORAGE DISEASE; HEREDITARY FRUCTOSE INTOLERANCE; HOMOCYSTINURIA; HUMAN; INBORN ERROR OF METABOLISM; MAPLE SYRUP URINE DISEASE; PHENYLKETONURIA; REVIEW; UREA CYCLE DISORDER;

EID: 80051924159     PISSN: 17517222     EISSN: 1878206X     Source Type: Journal    
DOI: 10.1016/j.paed.2011.04.006     Document Type: Review

References (4)

1. Emergency management protocols are available on the British Inherited Metabolic Disease Group website, http://www.bimdg.org.uk.
2. Inborn metabolic diseases 2006, Springer-Verlag, Heidelberg. 4th Edn. J. Fernandes, J.M. Saudubray, G. van den Berghe, J.H. Walter (Eds.).
3. NICE hypercholesterolaemia guidelines: http://www.nice.org.uk.
4. Clinical paediatric dietetics 2007, Blackwell, Oxford. 3rd Edn. V. Shaw, M. Lawson (Eds.).