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

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...

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Detalles Bibliográficos
Autores principales: Szpecht, Dawid, Gadzinowski, Janusz, Seremak-Mrozikiewicz, Agnieszka, Kurzawińska, Grażyna, Drews, Krzysztof, Szymankiewicz, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496967/
https://www.ncbi.nlm.nih.gov/pubmed/28578513
http://dx.doi.org/10.1007/s00381-017-3460-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496967/
https://www.ncbi.nlm.nih.gov/pubmed/28578513
http://dx.doi.org/10.1007/s00381-017-3460-8

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