Article
The role of FV 1691G>A, FII 20210G>A mutations and MTHFR 677C>T; 1298A>C and 103G>T FXIII gene polymorphisms in pathogenesis of intraventricular hemorrhage in infants born before 32 weeks of gestation.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery - 1 Jul 2017
Szpecht Dawid, Gadzinowski Janusz, Seremak-Mrozikiewicz Agnieszka, Kurzawińska Grażyna, Drews Krzysztof, Szymankiewicz Marta
Abstract excerpt
BACKGROUND: Congenital thrombophilia is associated with an increased intraventricular hemorrhage (IVH) risk among newborns, but it may also play a protective role. The role of genetic polymorphisms involved in the coagulation pathway of IVH pathogenesis is probably a consequence of an increased risk of thrombosis in the fine blood vessels in the germinal matrix region. MATERIAL AND METHODS: The aim of this study...
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