[Serum lipoproteins in the generalized form of type III glycogenosis]
- PMID: 210590
[Serum lipoproteins in the generalized form of type III glycogenosis]
Abstract
Distinct accumulation of glycogen, anomalous in structure, and absence of amylo-1,6-glucosidase activity were observed in studies of material obtained by biopsy from liver and muscle tissues of a patient with generalized form of glycogenosis type III. Anamalous glycogen (limitdextrin) was also found in erythrocytes. Concentration of lipoproteins, especially of low density lipoproteins 12.20 S and 0-12 S, was increased in blood serum. Spectrum of lipoproteins acquired a tendency to normalization simultaneously with clinical improvement after intravenous administration of glucose and treatment with cholesterolamine per os.
Similar articles
-
[Study of glycogen metabolism in the liver in type III glycogenosis (limit dextrinosis)].Vopr Med Khim. 1975 Mar-Apr;21(2):162-5. Vopr Med Khim. 1975. PMID: 166513 Russian.
-
Accumulation of glycogen in sural nerve axons in adult-onset type III glycogenosis.Ann Neurol. 1986 Mar;19(3):294-7. doi: 10.1002/ana.410190313. Ann Neurol. 1986. PMID: 3457549
-
[Glycogen storage disease by amylo 1,6-glucosidase deficiency (author's transl)].An Esp Pediatr. 1980 Oct;13(10):901-8. An Esp Pediatr. 1980. PMID: 6937153 Spanish.
-
Glycogen storage disease.Semin Liver Dis. 1982 Nov;2(4):291-301. doi: 10.1055/s-2008-1040716. Semin Liver Dis. 1982. PMID: 6763342 Review. No abstract available.
-
[Glycogenosis type III. New aspects in nutritional management].An Esp Pediatr. 1991 Sep;35(3):211-3. An Esp Pediatr. 1991. PMID: 1741583 Review. Spanish. No abstract available.