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Gewählte Publikation:

Nowak-Göttl, U; Auberger, K; Göbel, U; Kreuz, W; Schneppenheim, R; Vielhaber, H; Zenz, W; Zieger, B.
Inherited defects of the protein C anticoagulant system in childhood thrombo-embolism.
Eur J Pediatr. 1996; 155(11):921-927 Doi: 10.1007/BF02282879
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Co-Autor*innen der Med Uni Graz
Zenz Werner
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Abstract:
Childhood thrombo-embolism is mostly the result of inherited thrombophilia or vascular insults combined with risk factors such as peripartal asphyxia, fetopathia diabetica, exsiccosis, septicaemia, central lines, congenital heart disease, cancer, trauma, surgery or elevated antiphospholipid antibodies. Inherited thrombophilia includes mainly defects of the protein C pathway, resistance to activated protein C, protein C or protein S deficiency. Resistance to activated protein C, in the majority of cases caused by the point mutation Arg 506 Gln of the factor V gene, has emerged as the most important hereditary cause of thrombo-embolism in adults and children. However, since an acquired risk of thrombo-embolic complications frequently masks the inherited deficiency in affected children, children with thrombo-embolism should have adequate laboratory evaluation for inherited coagulation disorders, especially the protein C pathway. Until more data on childhood thrombo-embolism are available, treatment recommendations will continue to be extrapolated from guidelines for adults.
Find related publications in this database (using NLM MeSH Indexing)
Blood Coagulation - physiology
Blood Coagulation Disorders - diagnosis
Child - diagnosis
Genetic Screening - diagnosis
Genotype - diagnosis
Heterozygote - diagnosis
Humans - diagnosis
Mutation - diagnosis
Phenotype - diagnosis
Protein C - genetics
Protein C Deficiency - genetics
Thromboembolism - genetics

Find related publications in this database (Keywords)
Resistance to Activated Protein C (Apcr)
Protein C
Protein S
Childhood Thromboembolism
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