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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mattioli 1885
2019
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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) |
format | Online Article Text |
id | pubmed-7233636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Mattioli 1885 |
record_format | MEDLINE/PubMed |
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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