Surdocardiac syndrome of Jervell and Lange-Nielsen, with prolonged QT interval present at birth, and severe anaemia and syncopal attacks in childhood
A case of the surdocardiac syndrome of Jervell and Lange-Nielsen, with prolonged QT interval in the electrocardiogram at birth, is described. The affected girl presented 3 1/2 years later with severe iron deficiency anaemia, despite apparently adequate nutrition. At the age of 4 1/2 years she had a...
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Veröffentlicht in: | British Heart Journal 1975-08, Vol.37 (8), p.830-832 |
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description | A case of the surdocardiac syndrome of Jervell and Lange-Nielsen, with prolonged QT interval in the electrocardiogram at birth, is described. The affected girl presented 3 1/2 years later with severe iron deficiency anaemia, despite apparently adequate nutrition. At the age of 4 1/2 years she had a sudden attack of unconsciousness. Treatment with the beta-adrenoceptor blocker practolol was started and 3 years after initiation of this treatment she has been free from syncopal attacks. The QT interval remains prolonged. Her brother also had severe iron deficiency anaemia and had several attacks of unconsciousness before he died suddenly at the age of 3 1/2 years. |
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The affected girl presented 3 1/2 years later with severe iron deficiency anaemia, despite apparently adequate nutrition. At the age of 4 1/2 years she had a sudden attack of unconsciousness. Treatment with the beta-adrenoceptor blocker practolol was started and 3 years after initiation of this treatment she has been free from syncopal attacks. The QT interval remains prolonged. 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The affected girl presented 3 1/2 years later with severe iron deficiency anaemia, despite apparently adequate nutrition. At the age of 4 1/2 years she had a sudden attack of unconsciousness. Treatment with the beta-adrenoceptor blocker practolol was started and 3 years after initiation of this treatment she has been free from syncopal attacks. The QT interval remains prolonged. Her brother also had severe iron deficiency anaemia and had several attacks of unconsciousness before he died suddenly at the age of 3 1/2 years.</description><subject>1-Propanol - therapeutic use</subject><subject>Anemia, Hypochromic - etiology</subject><subject>Anemia, Hypochromic - genetics</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Deafness - complications</subject><subject>Deafness - congenital</subject><subject>Electrocardiography</subject><subject>Female</subject><subject>Heart Diseases - complications</subject><subject>Heart Diseases - physiopathology</subject><subject>Heart Rate - drug effects</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Iron - administration & dosage</subject><subject>Practolol - therapeutic use</subject><subject>Syncope - complications</subject><subject>Syncope - drug therapy</subject><subject>Syncope - etiology</subject><subject>Syndrome</subject><issn>0007-0769</issn><issn>1355-6037</issn><issn>1468-201X</issn><issn>2053-5864</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1975</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kU2P0zAQhiMEWsrCjSuSJSS4NMWOHTs-7AGVb1VFLAviZk1id-NuEhfbKfSH8H9xyWr5OHDyeN7nnRl7suwhwQtCKH_W-rigYlEtKopvZTPCeJUXmHy5nc0wxiLHgsu72b0QtunKZMVPshNCJGGMzrIfH0evXQNeW2hQOAzau94gt0HvjN-brkMwaLSC4dLka2u6YIY5-mZji3bedS6lNfpwgewQEw5dypqERAQR1dbHdv7LH8zeeJNCML2FKXUYGrdLDogRmquQSqCmtZ1undP3szsbSL0eXJ-n2adXLy-Wb_LV-9dvl89Xec0Ej3lRyg2A1HWDay7LogaGNdYECqIBCi5Khgu8abRmlGBCTUVSKAxIerTW9DQ7m-ruxro3ukmTe-jUztse_EE5sOpvZbCtunR7xaqiqorkf3Lt9-7raEJUvQ1N-jUYjBuDShvhkvIj-PgfcOtGP6S3KSIExpJJXCZqPlGNdyF4s7mZhGB13LVKu1ZUqOpYOeGP_pz-NzwtN-n5pNsQzfcbGfyV4oKKUq0_LxWma3Z-Toh6kfinE1_32_93_gmb1cQM</recordid><startdate>19750801</startdate><enddate>19750801</enddate><creator>Langslet, A</creator><creator>Sorland, S J</creator><general>BMJ Publishing Group Ltd and British Cardiovascular Society</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19750801</creationdate><title>Surdocardiac syndrome of Jervell and Lange-Nielsen, with prolonged QT interval present at birth, and severe anaemia and syncopal attacks in childhood</title><author>Langslet, A ; Sorland, S J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b476t-259faa9dbc0b6952ba40d0d1a21daa26754020fcdd431013e81dd47ea93259fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1975</creationdate><topic>1-Propanol - therapeutic use</topic><topic>Anemia, Hypochromic - etiology</topic><topic>Anemia, Hypochromic - genetics</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Deafness - complications</topic><topic>Deafness - congenital</topic><topic>Electrocardiography</topic><topic>Female</topic><topic>Heart Diseases - complications</topic><topic>Heart Diseases - physiopathology</topic><topic>Heart Rate - drug effects</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Iron - administration & dosage</topic><topic>Practolol - therapeutic use</topic><topic>Syncope - complications</topic><topic>Syncope - drug therapy</topic><topic>Syncope - etiology</topic><topic>Syndrome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Langslet, A</creatorcontrib><creatorcontrib>Sorland, S J</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British Heart Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Langslet, A</au><au>Sorland, S J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surdocardiac syndrome of Jervell and Lange-Nielsen, with prolonged QT interval present at birth, and severe anaemia and syncopal attacks in childhood</atitle><jtitle>British Heart Journal</jtitle><addtitle>Br Heart J</addtitle><date>1975-08-01</date><risdate>1975</risdate><volume>37</volume><issue>8</issue><spage>830</spage><epage>832</epage><pages>830-832</pages><issn>0007-0769</issn><issn>1355-6037</issn><eissn>1468-201X</eissn><eissn>2053-5864</eissn><abstract>A case of the surdocardiac syndrome of Jervell and Lange-Nielsen, with prolonged QT interval in the electrocardiogram at birth, is described. The affected girl presented 3 1/2 years later with severe iron deficiency anaemia, despite apparently adequate nutrition. At the age of 4 1/2 years she had a sudden attack of unconsciousness. Treatment with the beta-adrenoceptor blocker practolol was started and 3 years after initiation of this treatment she has been free from syncopal attacks. The QT interval remains prolonged. Her brother also had severe iron deficiency anaemia and had several attacks of unconsciousness before he died suddenly at the age of 3 1/2 years.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and British Cardiovascular Society</pub><pmid>1191443</pmid><doi>10.1136/hrt.37.8.830</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 1-Propanol - therapeutic use Anemia, Hypochromic - etiology Anemia, Hypochromic - genetics Child Child, Preschool Deafness - complications Deafness - congenital Electrocardiography Female Heart Diseases - complications Heart Diseases - physiopathology Heart Rate - drug effects Humans Infant, Newborn Iron - administration & dosage Practolol - therapeutic use Syncope - complications Syncope - drug therapy Syncope - etiology Syndrome |
title | Surdocardiac syndrome of Jervell and Lange-Nielsen, with prolonged QT interval present at birth, and severe anaemia and syncopal attacks in childhood |
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