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Hereditary thrombophilia

Thrombophilia is a group of disorders in which blood has an increased tendency to clot. It may be caused by inherited or acquired conditions. Thrombophilia is associated with risk of deep venous thrombosis and/or venous thromboembolism. Factor V Leiden thrombophilia is the most common inherited form...

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Autores principales: Dautaj, Astrit, Krasi, Geraldo, Bushati, Vilma, Precone, Vincenza, Gheza, Miriam, Fioretti, Francesco, Sartori, Marianna, Costantini, Alisia, Benedetti, Sabrina, Bertelli, Matteo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7233636/
https://www.ncbi.nlm.nih.gov/pubmed/31577252
http://dx.doi.org/10.23750/abm.v90i10-S.8758
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author Dautaj, Astrit
Krasi, Geraldo
Bushati, Vilma
Precone, Vincenza
Gheza, Miriam
Fioretti, Francesco
Sartori, Marianna
Costantini, Alisia
Benedetti, Sabrina
Bertelli, Matteo
author_facet Dautaj, Astrit
Krasi, Geraldo
Bushati, Vilma
Precone, Vincenza
Gheza, Miriam
Fioretti, Francesco
Sartori, Marianna
Costantini, Alisia
Benedetti, Sabrina
Bertelli, Matteo
author_sort Dautaj, Astrit
collection PubMed
description Thrombophilia is a group of disorders in which blood has an increased tendency to clot. It may be caused by inherited or acquired conditions. Thrombophilia is associated with risk of deep venous thrombosis and/or venous thromboembolism. Factor V Leiden thrombophilia is the most common inherited form of thrombophilia and prothrombin-related thrombophilia is the second most common genetic form of thrombophilia, occurring in about 1.7-3% of the European and US general populations (3). Thrombophilia may have autosomal dominant, autosomal recessive or X-linked inheritance. Genetic testing is useful for confirming diagnosis and for differential diagnosis, recurrence risk evaluation and asymptomatic diagnosis in families with a known mutation. (www.actabiomedica.it)
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spelling pubmed-72336362020-05-19 Hereditary thrombophilia Dautaj, Astrit Krasi, Geraldo Bushati, Vilma Precone, Vincenza Gheza, Miriam Fioretti, Francesco Sartori, Marianna Costantini, Alisia Benedetti, Sabrina Bertelli, Matteo Acta Biomed Review Thrombophilia is a group of disorders in which blood has an increased tendency to clot. It may be caused by inherited or acquired conditions. Thrombophilia is associated with risk of deep venous thrombosis and/or venous thromboembolism. Factor V Leiden thrombophilia is the most common inherited form of thrombophilia and prothrombin-related thrombophilia is the second most common genetic form of thrombophilia, occurring in about 1.7-3% of the European and US general populations (3). Thrombophilia may have autosomal dominant, autosomal recessive or X-linked inheritance. Genetic testing is useful for confirming diagnosis and for differential diagnosis, recurrence risk evaluation and asymptomatic diagnosis in families with a known mutation. (www.actabiomedica.it) Mattioli 1885 2019 2019-09-30 /pmc/articles/PMC7233636/ /pubmed/31577252 http://dx.doi.org/10.23750/abm.v90i10-S.8758 Text en Copyright: © 2019 ACTA BIO MEDICA SOCIETY OF MEDICINE AND NATURAL SCIENCES OF PARMA http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution 4.0 International License
spellingShingle Review
Dautaj, Astrit
Krasi, Geraldo
Bushati, Vilma
Precone, Vincenza
Gheza, Miriam
Fioretti, Francesco
Sartori, Marianna
Costantini, Alisia
Benedetti, Sabrina
Bertelli, Matteo
Hereditary thrombophilia
title Hereditary thrombophilia
title_full Hereditary thrombophilia
title_fullStr Hereditary thrombophilia
title_full_unstemmed Hereditary thrombophilia
title_short Hereditary thrombophilia
title_sort hereditary thrombophilia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7233636/
https://www.ncbi.nlm.nih.gov/pubmed/31577252
http://dx.doi.org/10.23750/abm.v90i10-S.8758
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