Haemostatic Studies in Carbohydrate-deficient Glycoprotein Syndrome Type I

Author:

Fiumara A1,Barone R1,Buttitta P2,Musso R3,Pavone L1,Nigro F1,Jaeken J4

Affiliation:

1. Department of Paediatrics, University of Catania, Italy

2. The Department of Neonatology, G. Cristina Hospital, Palermo, Italy

3. Department of Hematology, Hemophilia Section, University of Catania, Italy

4. Department of Paediatrics, University of Leuven, Belgium

Abstract

SummaryCDG syndrome (CDGS) type I is the most frequent form of a group of metabolic disorders characterised by a defect of the carbohydrate moiety of glycoproteins. A large number of plasma glycoproteins, including clotting factors and inhibitors, are decreased and stroke-like episodes have been described in about half of the reported patients. We studied blood coagulation factors, inhibitors and D-dimer plasma levels in four subjects, aged 12-23 years, with CDGS type I. Factors VIII, XI, antithrombin III activity, antigen plasma levels of antithrombin III, free protein S and protein C were decreased whereas protein C as activity was normal. In addition two patients had reduction of factors II, V, VII, IX, X reflecting the phenotypic heterogeneity associated with CDGS type I. D-dimer plasma concentrations were elevated in all subjects. The hypercoagulable state as consequence of the combined deficiencies of coagulation inhibitors could contribute to the stroke-like phenomena in CDGS type I.

Publisher

Georg Thieme Verlag KG

Subject

Hematology

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1. Association between acute complications in PMM2-CDG patients and haemostasis anomalies: Data from a multicentric study and suggestions for acute management;Molecular Genetics and Metabolism;2023-11

2. Hemostatic defects in congenital disorders of glycosylation;Research and Practice in Thrombosis and Haemostasis;2023-03

3. Congenital disorders of N-linked glycosylation;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020

4. Elevated thrombin generation in patients with congenital disorder of glycosylation and combined coagulation factor deficiencies;Journal of Thrombosis and Haemostasis;2019-07-28

5. Factor VIII and vWF deficiency in STT3A‐CDG;Journal of Inherited Metabolic Disease;2019-01-30

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