Literature DB >> 6767011

Type I glycogen storage disease: five years of management with nocturnal intragastric feeding.

H L Greene, A E Slonim, I M Burr, J R Moran.   

Abstract

It has been five years since the original report indicating that intragastric feedings could reverse most of the clinical and metabolic abnormalities present in patients with type I glycogen storage disease. We have now treated seven patients with nocturnal intragastric feedings for five years. All patients have shown marked improvement in blood chemical values (urate, lactate, triglyceride, cholesterol) as well as linear growth. The only serious complication has been symptomatic hypoglycemia and acidosis resulting from acute gastroenteritis and vomiting. Results indicate that nocturnal intragastric feeding is a practical, safe, and effective form of long-term treatment for patients with type I glycogen storage disease.

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Year:  1980        PMID: 6767011     DOI: 10.1016/s0022-3476(80)80871-7

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  8 in total

1.  Glucose production rates in type 1 glycogen storage disease.

Authors:  J E Collins; K Bartlett; J V Leonard; A Aynsley-Green
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Glycogen storage disease type I. Results of treatment with frequent daytime feeding, combined with nocturnal intragastric feeding and with administration of an alpha-glucosidase inhibitor.

Authors:  H Gröbe; K Ullrich
Journal:  Eur J Pediatr       Date:  1983-04       Impact factor: 3.183

3.  Glycogenosis type Ib complicated by severe granulocytopenia resembling inherited neutropenia.

Authors:  C R Bartram; H Przyrembel; U Wendel; H J Bremer; J Schaub; J R Haas
Journal:  Eur J Pediatr       Date:  1981-09       Impact factor: 3.183

4.  Plasma and lipoprotein fatty acid composition in glycogen storage disease type I.

Authors:  E Levy; J Letarte; G Lepage; L Thibault; C C Roy
Journal:  Lipids       Date:  1987-06       Impact factor: 1.880

5.  Hyperuricemia in glycogen storage disease type I. Contributions by hypoglycemia and hyperglucagonemia to increased urate production.

Authors:  J L Cohen; A Vinik; J Faller; I H Fox
Journal:  J Clin Invest       Date:  1985-01       Impact factor: 14.808

6.  Effects of cornstarch treatment in very young children with type I glycogen storage disease.

Authors:  M Hayde; K Widhalm
Journal:  Eur J Pediatr       Date:  1990-06       Impact factor: 3.183

7.  Chronic pancreatitis in a child with glycogen storage disease type 1.

Authors:  M Kikuchi; K Hasegawa; I Handa; M Watabe; K Narisawa; K Tada
Journal:  Eur J Pediatr       Date:  1991-10       Impact factor: 3.183

Review 8.  The hepatic glycogen storage diseases--problems beyond childhood.

Authors:  P J Lee; J V Leonard
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

  8 in total

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