European Journal of Pediatrics

, Volume 139, Issue 3, pp 210–210 | Cite as

Phosphorylase kinase deficiency: Severe glycogen storage disease with evidence of autosomal recessive mode of inheritance

  • O. Søvik
  • Th. de Barsy
  • B. Maehle
Letters to the Editors

References

  1. Bashan N, Iancu TC, Lerner A, Fraset D, Potashnik R, Moses SW (1981) Glycogenosis due to liver and muscle phosphorylase kinase deficiency Pediatr Res 15:299–303PubMedGoogle Scholar
  2. Lederer B, van Hoof F, van den Berghe, Hers HG (1975) Glycogen phosphorylase and its converter enzymes in haemolysates of normal subjects and patients with type VI glycogen-storage disease. Biochem J 147: 23–35PubMedGoogle Scholar
  3. Lederer B, van de Werne G, deBarsy Th, Hers HG (1980) The autosomal form of phosphorylase kinase deficiency in man: Reduced activity of the muscle enzyme. Biochem Biophys Res Commun 92:169–174PubMedGoogle Scholar
  4. Mahler RF (1976) Disorders of glycogen metabolism. Clin Endocrinol Metab 5: 579–598PubMedGoogle Scholar

Copyright information

© Springer-Verlag 1982

Authors and Affiliations

  • O. Søvik
    • 1
  • Th. de Barsy
    • 3
  • B. Maehle
    • 2
  1. 1.Department of PediatricsUniversity of Bergen, 5016 Haukeland HospitalBergenNorway
  2. 2.Department of PathologyUniversity of Bergen, 5016 Haukeland HospitalBergenNorway
  3. 3.Laboratoire de Chimie PhysiologiqueUniversité Catholique de LouvainBrusselsBelgium

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