Recurrent thrombo-embolism in a child with a congenital disorder of glycosylation (CDG) type Ib and treatment with mannose

Pediatric Hematology and Oncology

Volumn 25, Issue 8, 2008, Pages 762-768

  Tamminga, R Y J ^a   Lefeber, D J ^b   Kamps, W A ^a   Van Spronsen, F J ^a  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

CDG; Coagulopathy; Congenital disorder of glycosylation; Jaeken syndrome; Mannose; Thrombosis

Indexed keywords

HEPARIN; LOW MOLECULAR WEIGHT HEPARIN; MANNOSE; MANNOSE PHOSPHATE ISOMERASE; TRANSFERRIN; WARFARIN;

ANTICOAGULANT THERAPY; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1B; DEEP VEIN THROMBOSIS; DOPPLER FLOWMETRY; FAMILY HISTORY; FEMALE; FEMORAL VEIN; GENE MUTATION; GENETIC ANALYSIS; HUMAN; ISOELECTRIC FOCUSING; LABORATORY TEST; LUNG EMBOLISM; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD; RECURRENT DISEASE; VEIN THROMBOSIS;

BLOOD COAGULATION FACTORS; CARBOHYDRATE METABOLISM, INBORN ERRORS; CHILD, PRESCHOOL; FEMALE; GLYCOSYLATION; HUMANS; MANNOSE; RECURRENCE; THROMBOEMBOLISM;

EID: 57449102405     PISSN: 08880018     EISSN: 15210669     Source Type: Journal    
DOI: 10.1080/08880010802394616     Document Type: Article

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