Factor V Leiden in Patients with recurrent Fetal Loss

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F00%3A00002625" target="_blank" >RIV/00216224:14110/00:00002625 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Factor V Leiden in Patients with recurrent Fetal Loss

Original language description

S u m m a r y: The factor V Leiden mutation is the most common genetic predisposition to thrombosis. Our purpose was to determine the association of Factor V Leiden mutation (FVL) frequency and recurrent fetal loss.We examined the prevalence of the pointmutation in the factor V gene (R 506 Q or Leiden) in 138 unselected women with a history of one or more spontaneous abortion or stillbirth of unexplained etiology. In our referral population women, a statistically significant association of the Leidenmutation with recurrent fetal losses was found. The risk for recurrence of fetal loss tended to be greater in homozygous carriers.

Czech name

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Czech description

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Type

D - Article in proceedings

CEP classification

EB - Genetics and molecular biology

OECD FORD branch

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Project

<a href="/en/project/VS96097" target="_blank" >VS96097: Molecular pathophysiology of selected multigenic related to civilization diseases</a><br>

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year

2000

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Article name in the collection

Book of Abstracts of XVI. FIGO World Congress

ISBN

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ISSN

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e-ISSN

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Number of pages

1

Pages from-to

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Publisher name

Congress of Gynecology and Obstetrics

Place of publication

Washington D.C.

Event location

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Event date

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Type of event by nationality

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UT code for WoS article

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