Symptomatic hyperinsulinism reversed by dietary manipulation in glycogenosis type III

Journal of Inherited Metabolic Disease

Volumn 20, Issue 4, 1997, Pages 612-613

  Lee, P J ^a,c   Ferguson, C ^b   Alexander, F W ^b  

^a ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^b NEWCASTLE GENERAL HOSPITAL   (United Kingdom)

^c GREAT ORMOND STREET HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSE; GLUCOSE POLYMER; GLYCOGEN; GLYCOGEN DEBRANCHING ENZYME; INSULIN; KETONE BODY;

ARTICLE; BODY HEIGHT; BODY WEIGHT; CARBOHYDRATE DIET; CASE REPORT; DIET SUPPLEMENTATION; DIET THERAPY; ENZYME DEFICIENCY; FEMALE; GLUCOSE BLOOD LEVEL; GLYCOGEN STORAGE DISEASE TYPE 3; HUMAN; HYPERINSULINISM; HYPOGLYCEMIA; INFANT; INSULIN BLOOD LEVEL; MILK; PRESCHOOL CHILD;

DIET THERAPY; FEMALE; GLYCOGEN STORAGE DISEASE TYPE III; HUMANS; HYPERINSULINISM; HYPOGLYCEMIA; INFANT;

EID: 0030837831     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005383831637     Document Type: Article

References (3)

1. Dunger DB, Sutton P, Leonard JV (1995) Hypoglycaemia complicating treatment regimens for glycogen storage disease. Arch Dis Child 72: 274-275.
2. Slonim AE, Coleman RA, Moses WS (1984) Myopathy and growth failure in debrancher enzyme deficiency: improvement with high protein nocturnal enterai therapy. J Pediatr 105: 906-911.
3. Stanley CA, Mills JL, Baker L (1981) Intragastric feeding in type I glycogen storage disease: factors affecting the control of lactic acidemia. Pediatr Res 15: 1504-1508.