BOVINE GENERALIZED GLYCOGENOSIS
- 1 January 1977
- journal article
- research article
- Published by Wiley in Neuropathology and Applied Neurobiology
- Vol. 3 (1), 45-56
- https://doi.org/10.1111/j.1365-2990.1977.tb00568.x
Abstract
The clinical, pathological, and biochemical features of a glycogen storage disease in beef cattle are described. The light and electron microscope changes in skeletal muscle, heart and the central nervous system were similar to the lesions that have been described in glycogenosis Type II, or Pompe's disease, in man. The stored intracytoplasmic material was shown histochemically and electron microscopically to be glycogen. Biochemical assay of liver, skeletal muscle, and heart demonstrated a deficiency of the lysosomal enzyme α‐1, 4‐glucosidase.This publication has 12 references indexed in Scilit:
- The pathology of type II skeletal muscle glycogenosis. A light and electron-microscopic studyThe Journal of Pathology, 1975
- Generalized glycogen storage disease in sheepJournal of Comparative Pathology, 1975
- Pompe's disease: An inborn lysosomal disorder with storage of glycogenActa Neuropathologica, 1973
- Inherited lysosomal storage diseases: an essay in comparative medicinePublished by Wiley ,1973
- A Case of Glycogenic Cardiomegaly in a DogActa Veterinaria Scandinavica, 1970
- Glycogenosis of the central nervous system in the catActa Neuropathologica, 1969
- FIELD PROCEDURE FOR COUNTING GASTRO‐INTESTINAL WORMS IN SHEEP AND CATTLE*Australian Veterinary Journal, 1967
- A HISTOCHEMICAL AND ELECTRON MICROSCOPIC STUDY OF SKELETAL MUSCLE IN A CASE OF POMPE'S DISEASE (GLYCOGENOSIS II)Pediatrics, 1966
- Inborn Lysosomal DiseasesGastroenterology, 1965
- α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)Biochemical Journal, 1963