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Article

Factor V Leiden and genetic defects of thrombophilia in childhood porencephaly

1 Mar 1998

Abstract excerpt

AIMS: To determine to what extent the Arg506 to Gln point mutation in the factor V gene and further genetic factors of thrombophilia affect the risk of porencephaly in neonates and infants. METHODS: The Arg506 to Gln mutation, factor V, protein C, protein S, antithrombin, antiphospholipid antibodies and lipoprotein (a) (Lp(a)) were retrospectively measured in neonates and children with porencephaly (n = 24)....

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PMID: 9577282
DOI: 10.1136/fn.78.2.f121

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