Hepatic Phosphorylase Defect
- 1 March 1966
- journal article
- research article
- Published by American Medical Association (AMA) in American Journal of Diseases of Children
- Vol. 111 (3) , 278-282
- https://doi.org/10.1001/archpedi.1966.02090060088008
Abstract
STUDIES OF THE genetics of glycogen storage disease have been hampered by the obvious difficulty of obtaining tissue from apparently healthy relatives for enzyme assays. In 1961, Williams and Field1 from the United States and Hülsmann et al2 from Belgium reported very low leukocyte phosphorylase activity in five patients with proven hepatic phosphorylase defect. In two of the families there was also low leukocyte phosphorylase activity in the mother, but normal values in the father and male siblings. The mothers were quite healthy in both instances and a sex-linked, dominant form of inheritance was postulated by both sets of authors. Sidbury et al3,4 have studied the erythrocyte glycogen concentration and its β-amylase degradation in many cases of glycogen storage disease. High concentrations were found in limit dextrinosis and in hepatic phosphorylase defect. Abnormally short and long chain structure of glycogen could be demonstrated. These peripheral blood studiesThis publication has 0 references indexed in Scilit: