SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM

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Main Authors: Zohreh Rahimi, Abbas Parsian
Format: Article
Language:English
Published: PAGEPress Publications 2011-01-01
Series:Mediterranean Journal of Hematology and Infectious Diseases
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Online Access:http://www.mjhid.org/article/view/7909
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author Zohreh Rahimi
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mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin:0cm; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;} </style> <![endif]--> <p class="MsoNormal" style="text-align: justify; line-height: 200%; direction: ltr; unicode-bidi: embed;"><span style="color: black;" lang="EN-US">Hemoglobin S in homozygous state or in combination with one of the structural variants of Hb </span><span style="color: black;" lang="EN-US">D-Punjab, Hb O-Arab, Hb C or β-thalassemia mutation</span><span style="color: black;" lang="EN-US"> results in sickle cell disease (SCD) that is characterized by chronic hemolytic anemia and tissue injury secondary to vasooclusion. A chronic hypercoagulable state in SCD has been established with the increased risk of thromboembolic complications in these patients. The goal of present review is to survey of the literature related to thromboembolic events and genetic risk factors involved in the manifestation of these events in SCD patients with focus on studies from Mediterranean countries. Also, this review covers the pathogenesis of hypercoagulability and alteration in the components of hemostasis system.</span></p>
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QFormat="true" Name="TOC Heading" /> </w:LatentStyles> </xml><![endif]--><!--[if gte mso 10]> <style> /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Tabella normale"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin:0cm; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;} </style> <![endif]--> <p class="MsoNormal" style="text-align: justify; line-height: 200%; direction: ltr; unicode-bidi: embed;"><span style="color: black;" lang="EN-US">Hemoglobin S in homozygous state or in combination with one of the structural variants of Hb </span><span style="color: black;" lang="EN-US">D-Punjab, Hb O-Arab, Hb C or β-thalassemia mutation</span><span style="color: black;" lang="EN-US"> results in sickle cell disease (SCD) that is characterized by chronic hemolytic anemia and tissue injury secondary to vasooclusion. A chronic hypercoagulable state in SCD has been established with the increased risk of thromboembolic complications in these patients. The goal of present review is to survey of the literature related to thromboembolic events and genetic risk factors involved in the manifestation of these events in SCD patients with focus on studies from Mediterranean countries. Also, this review covers the pathogenesis of hypercoagulability and alteration in the components of hemostasis system.</span></p>http://www.mjhid.org/article/view/7909Sickle cell , Anemia, Thrombosisi, Venous occlusion
spellingShingle Zohreh Rahimi
Abbas Parsian
SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM
Mediterranean Journal of Hematology and Infectious Diseases
Sickle cell , Anemia, Thrombosisi, Venous occlusion
title SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM
title_full SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM
title_fullStr SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM
title_full_unstemmed SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM
title_short SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM
title_sort sickle cell disease and venous thromboembolism
topic Sickle cell , Anemia, Thrombosisi, Venous occlusion
url http://www.mjhid.org/article/view/7909
work_keys_str_mv AT zohrehrahimi sicklecelldiseaseandvenousthromboembolism
AT abbasparsian sicklecelldiseaseandvenousthromboembolism