Glycogen Storage Disease Type Ia in Two Littermate Maltese Puppies
Open Access
- 1 September 1995
- journal article
- research article
- Published by SAGE Publications in Veterinary Pathology
- Vol. 32 (5) , 460-465
- https://doi.org/10.1177/030098589503200502
Abstract
Glycogen storage disease type Ia (GSD-Ia) (von Gierke's disease) was identified in two 47-day-old littermate Maltese puppies. The puppies were presented for necropsy with a history of failure to thrive, mental depression, and poor body condition. Gross findings included small body size and emaciation (212 and 246 g versus 595 g for normal littermate), severely enlarged pale livers (48 and 61 g), and pale kidneys. Histologically, there was marked diffuse vacuolation of hepatocytes with large amounts of glycogen and small amounts of lipid. Renal tubular epithelium was mildly to moderately vacuolated. Soft tissue mineralization was present in renal tubules and pulmonary alveolar septa. Biochemical analysis showed that levels of glucose-6-phosphatase were markedly reduced in liver (0.3 and 0.4 μM/minute/g tissue versus 4.7 ± 1.5 μM/minute/g tissue for controls) and kidney (0.45 and 0.4 μM/minute/g tissue versus 4.1 μM/minute/g tissue for controls) and that glycogen content was increased in liver (9.4% and 9.4% versus 1.3% ± 1.4% for controls). This is the first confirmed report of animals with glycogen storage disease type Ia.Keywords
This publication has 21 references indexed in Scilit:
- Renal complications in glycogen storage disease type IEuropean Journal of Pediatrics, 1993
- Human microsomal glucose-6-phosphatase systemEuropean Journal of Pediatrics, 1993
- Glucose-6-phosphate: A key compound in glycogenosis I and favism leading to hyper- or hypolipidaemiaEuropean Journal of Pediatrics, 1993
- Glycogen storage disease I and hepatocellular tumoursEuropean Journal of Pediatrics, 1993
- The long-term outcome of patients with glycogen storage disease type IaEuropean Journal of Pediatrics, 1993
- Type I glycogen storage disease: Nine years of management with cornstarchEuropean Journal of Pediatrics, 1993
- Renal Disease in Type I Glycogen Storage DiseaseNew England Journal of Medicine, 1988
- Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiencyMetabolism, 1986
- Liver‐specific glucose‐6‐phosphatase is not present in human placentaJournal of Inherited Metabolic Disease, 1984
- Cornstarch Therapy in Type I Glycogen-Storage DiseaseNew England Journal of Medicine, 1984