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Two New Examples of Hb St. Etienne [β 92(F8)His→Gln] in Association with Venous Thrombosis
Hb St. Etienne [β92(F8)His→Gln] (also known as Hb Istanbul) is a rare unstable β-globin chain variant that has been described in only three reports involving four patients. We report two individuals in a family of Scottish extraction whose members had been erroneously diagnosed to have hereditary sp...
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Published in: | Hemoglobin 2009, Vol.33 (2), p.95-100 |
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container_title | Hemoglobin |
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creator | Au, Nicholas H.C. Wong, Ann Y.K. Vickars, Linda MacGillivray, Ross T.A. Wadsworth, Louis D. |
description | Hb St. Etienne [β92(F8)His→Gln] (also known as Hb Istanbul) is a rare unstable β-globin chain variant that has been described in only three reports involving four patients. We report two individuals in a family of Scottish extraction whose members had been erroneously diagnosed to have hereditary spherocytosis (HS) and have now been shown to be heterozygotes for Hb St. Etienne. They also had venous thrombotic events with minimal provocation. This family illustrates the difficulties in identifying the cause of chronic hemolytic anemia and highlights the possible contribution of chronic hemolysis to increased risk of thrombosis. |
doi_str_mv | 10.1080/03630260902817206 |
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We report two individuals in a family of Scottish extraction whose members had been erroneously diagnosed to have hereditary spherocytosis (HS) and have now been shown to be heterozygotes for Hb St. Etienne. They also had venous thrombotic events with minimal provocation. This family illustrates the difficulties in identifying the cause of chronic hemolytic anemia and highlights the possible contribution of chronic hemolysis to increased risk of thrombosis.</description><identifier>ISSN: 0363-0269</identifier><identifier>EISSN: 1532-432X</identifier><identifier>DOI: 10.1080/03630260902817206</identifier><identifier>PMID: 19373584</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Adolescent ; Base Sequence ; DNA Mutational Analysis ; Female ; Hb Istanbul ; Hb St. Etienne ; Hemoglobinopathies ; Hemoglobins, Abnormal - genetics ; Hemolytic anemia ; Heterozygote ; Humans ; Male ; Middle Aged ; Molecular Sequence Data ; Scotland ; Spherocytosis, Hereditary - diagnosis ; Unstable hemoglobin (Hb) ; Veno-occlusive disease ; Venous Thrombosis - genetics</subject><ispartof>Hemoglobin, 2009, Vol.33 (2), p.95-100</ispartof><rights>2009 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-730ddb57a5f4585be21bdbb4762013301b57a61e247da20bef216bc69b03c523</citedby><cites>FETCH-LOGICAL-c404t-730ddb57a5f4585be21bdbb4762013301b57a61e247da20bef216bc69b03c523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19373584$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Au, Nicholas H.C.</creatorcontrib><creatorcontrib>Wong, Ann Y.K.</creatorcontrib><creatorcontrib>Vickars, Linda</creatorcontrib><creatorcontrib>MacGillivray, Ross T.A.</creatorcontrib><creatorcontrib>Wadsworth, Louis D.</creatorcontrib><title>Two New Examples of Hb St. Etienne [β 92(F8)His→Gln] in Association with Venous Thrombosis</title><title>Hemoglobin</title><addtitle>Hemoglobin</addtitle><description>Hb St. Etienne [β92(F8)His→Gln] (also known as Hb Istanbul) is a rare unstable β-globin chain variant that has been described in only three reports involving four patients. 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This family illustrates the difficulties in identifying the cause of chronic hemolytic anemia and highlights the possible contribution of chronic hemolysis to increased risk of thrombosis.</description><subject>Adolescent</subject><subject>Base Sequence</subject><subject>DNA Mutational Analysis</subject><subject>Female</subject><subject>Hb Istanbul</subject><subject>Hb St. Etienne</subject><subject>Hemoglobinopathies</subject><subject>Hemoglobins, Abnormal - genetics</subject><subject>Hemolytic anemia</subject><subject>Heterozygote</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Molecular Sequence Data</subject><subject>Scotland</subject><subject>Spherocytosis, Hereditary - diagnosis</subject><subject>Unstable hemoglobin (Hb)</subject><subject>Veno-occlusive disease</subject><subject>Venous Thrombosis - genetics</subject><issn>0363-0269</issn><issn>1532-432X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kE1KAzEYhoMoWn8O4EayEl2MfvmZP3RTpFpBdGERQSQkMxkamUlqMqV6AQ_gUTyIh_AkTmlBRHD1Ld7nffl4ENolcEQgg2NgCQOaQA40IymFZAX1SMxoxBm9X0W9eR51QL6BNkN4AiB5CnwdbZCcpSzOeA89jmYOX-sZHrzIZlLrgF2Fhwrftkd40BptrcYPnx84pwfn2eHQhK-394vaPmJjcT8EVxjZGmfxzLRjfKetmwY8GnvXKBdM2EZrlayD3lneLTQ6H4zOhtHVzcXlWf8qKjjwNkoZlKWKUxlXPM5ipSlRpVI8TSgQxoDMs4RoytNSUlC6oiRRRZIrYEVM2RbaX8xOvHue6tCKxoRC17W0untIJClhnNC4A8kCLLwLwetKTLxppH8VBMRcqfijtOvsLcenqtHlT2PpsANOF4CxlfONnDlfl6KVr7XzlZe2MEGw__ZPftXHWtbtuJBeiyc39bbz9s9336OuldM</recordid><startdate>2009</startdate><enddate>2009</enddate><creator>Au, Nicholas H.C.</creator><creator>Wong, Ann Y.K.</creator><creator>Vickars, Linda</creator><creator>MacGillivray, Ross T.A.</creator><creator>Wadsworth, Louis D.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2009</creationdate><title>Two New Examples of Hb St. Etienne [β 92(F8)His→Gln] in Association with Venous Thrombosis</title><author>Au, Nicholas H.C. ; Wong, Ann Y.K. ; Vickars, Linda ; MacGillivray, Ross T.A. ; Wadsworth, Louis D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-730ddb57a5f4585be21bdbb4762013301b57a61e247da20bef216bc69b03c523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Base Sequence</topic><topic>DNA Mutational Analysis</topic><topic>Female</topic><topic>Hb Istanbul</topic><topic>Hb St. Etienne</topic><topic>Hemoglobinopathies</topic><topic>Hemoglobins, Abnormal - genetics</topic><topic>Hemolytic anemia</topic><topic>Heterozygote</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Molecular Sequence Data</topic><topic>Scotland</topic><topic>Spherocytosis, Hereditary - diagnosis</topic><topic>Unstable hemoglobin (Hb)</topic><topic>Veno-occlusive disease</topic><topic>Venous Thrombosis - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Au, Nicholas H.C.</creatorcontrib><creatorcontrib>Wong, Ann Y.K.</creatorcontrib><creatorcontrib>Vickars, Linda</creatorcontrib><creatorcontrib>MacGillivray, Ross T.A.</creatorcontrib><creatorcontrib>Wadsworth, Louis D.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Hemoglobin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Au, Nicholas H.C.</au><au>Wong, Ann Y.K.</au><au>Vickars, Linda</au><au>MacGillivray, Ross T.A.</au><au>Wadsworth, Louis D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two New Examples of Hb St. Etienne [β 92(F8)His→Gln] in Association with Venous Thrombosis</atitle><jtitle>Hemoglobin</jtitle><addtitle>Hemoglobin</addtitle><date>2009</date><risdate>2009</risdate><volume>33</volume><issue>2</issue><spage>95</spage><epage>100</epage><pages>95-100</pages><issn>0363-0269</issn><eissn>1532-432X</eissn><abstract>Hb St. Etienne [β92(F8)His→Gln] (also known as Hb Istanbul) is a rare unstable β-globin chain variant that has been described in only three reports involving four patients. We report two individuals in a family of Scottish extraction whose members had been erroneously diagnosed to have hereditary spherocytosis (HS) and have now been shown to be heterozygotes for Hb St. Etienne. They also had venous thrombotic events with minimal provocation. This family illustrates the difficulties in identifying the cause of chronic hemolytic anemia and highlights the possible contribution of chronic hemolysis to increased risk of thrombosis.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>19373584</pmid><doi>10.1080/03630260902817206</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Base Sequence DNA Mutational Analysis Female Hb Istanbul Hb St. Etienne Hemoglobinopathies Hemoglobins, Abnormal - genetics Hemolytic anemia Heterozygote Humans Male Middle Aged Molecular Sequence Data Scotland Spherocytosis, Hereditary - diagnosis Unstable hemoglobin (Hb) Veno-occlusive disease Venous Thrombosis - genetics |
title | Two New Examples of Hb St. Etienne [β 92(F8)His→Gln] in Association with Venous Thrombosis |
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