Abstract
This paper concerns the clinical and biochemical course in two siblings with glucose-6-phosphatase deficiency, who have been treated with supplementary glucose according to a variety of regimes.
This is a preview of subscription content, log in via an institution to check access.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Similar content being viewed by others
References
G. Ball, L. Chenery, D. Hemsley and A. J. Macnab, (1974). A miniature peristaltic pump with electronic rate control: technical adaption to a clinical need. Biomedical Engineering, 9, 563
R. A. Hutton, A. J. Macnab and R. P. A. Rivers, (1976). Defect of platelet function associated with chronic hypoglycemia. Arch. Dis. Child., 51, 49
A. J. Macnab, (1974). Type 1 glycogenosis: effects of prolonged intravenous dextrose infusion on growth and plasma biochemistry. Pediatr. Res., 8, 136
A. J. Macnab, (1974). Increased growth velocity in type 1 glycogen storage disease during reversal of metabolic abnormalities by two periods of prolonged dextrose infusion. Pediatrica XIV: Proceedings of 14th International Congress of Paediatrics, 10 (Metabolism), p. 195
T. E. Starzl C. W. Putna K. A. Porter C. G. Halgrimson J. Corman B. I. Brown R. W. Gotlin D. D. Rodgerson and H. L. Green 1973. Portal diversion for the treatment of glycogen storage disease in humans. Ann. Surg. 178 52
J. Folkman, A. Philippart, W-J Tze and J. Crigler, (1972). Portacaval shunt for glycogen storage disease: value of prolonged intravenous hyperalimentation before surgery. Surgery, 72, 306
H. L. Greene, A. E. Slonim, J. A. O’Neill and I. M. Burr, (1976). Continuous nasogastric feeding for management of type 1 glycogen storage disease. N. Engl. J. Med., 294, 423
I. M. Burr, J. A. O’Neill, D. T. Karzon, L. J. Howard and H. L. Green, (1974). Comparison of the effects of total parenteral nutrition, continuous intragastric feeding, and portacaval shunt on a patient with type 1 glycogen storage disease. J. Pediatr., 85, 792
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1980 The Society for the Study of Inborn Errors of Metabolism
About this chapter
Cite this chapter
Stacey, T.E., Macnab, A., Strang, L.B. (1980). Recent work on treatment of Type I glycogen storage disease. In: Burman, D., Holton, J.B., Pennock, C.A. (eds) Inherited Disorders of Carbohydrate Metabolism. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-9215-3_19
Download citation
DOI: https://doi.org/10.1007/978-94-009-9215-3_19
Publisher Name: Springer, Dordrecht
Print ISBN: 978-94-009-9217-7
Online ISBN: 978-94-009-9215-3
eBook Packages: Springer Book Archive