Decreased blood coagulation activities in carbohydrate‐deficient glycoprotein syndrome
- 1 March 1993
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 16 (2), 435-440
- https://doi.org/10.1007/bf00710294
Abstract
The carbohydrate-deficient glycoprotein (CDG) syndromes are a newly recognized group of inherited metabolic diseases. We report a Japanese brother and sister with a CDG syndrome. Both patients showed decreased activities of blood coagulation Factor XI and of the coagulation inhibitor protein C. In one of them there was also a somewhat decreased activity of Factor IX and of antithrombin III. Isoelectric focusing of antithrombin III revealed a decrease of negatively charged fractions and an increase of more cathodal bands. Furthermore, there was a discrepancy between activity and antigen level of Factor VIII and protein C. The patients had an incidental deficiency of factor XII. This is the first detailed report on blood coagulation systems in the CDG syndromes. These blood coagulation abnormalities may explain at least in part the thrombotic or haemorrhagic complications of the CDG syndromes.Keywords
This publication has 9 references indexed in Scilit:
- The carbohydrate deficient glycoprotein syndrome in three Japanese childrenBrain & Development, 1992
- A new variant of the carbohydrate deficient glycoproteins syndromeJournal of Inherited Metabolic Disease, 1991
- Biochemical Characteristics and Diagnosis of the Carbohydrate‐deficient Glycoprotein SyndromeActa Paediatrica, 1991
- Carbohydrate deficient serum transferrin in a new systemic hereditary syndrome.Archives of Disease in Childhood, 1990
- Disialotransferrin developmental deficiency syndrome.Archives of Disease in Childhood, 1989
- Development of the human coagulation system in the full-term infantBlood, 1987
- Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndromeClinica Chimica Acta; International Journal of Clinical Chemistry, 1984
- A new procedure for the determination of transferrinC (TfC) subtypes by isoelectric focusingHuman Genetics, 1980
- Familial psychomotor retardation with markedly fluctuating serum prolactin, FSH and GH levels, partial TBG-deficiency, increased serum arylsulphatase A and increased CSF protein: a new syndrome?: 90Pediatric Research, 1980