Unclassified sudden infant death due to congenital long QT syndrome with TRPM4 mutation
Background: Congenital long QT syndrome (cLQTS) are heritable disorders due to genetic mutations causing prolonged corrected QT (QTc) interval that may result in fatal arrhythmias. Clinical Description: A well 20-day-old, exclusively breastfed boy had an episode of unresponsiveness with no other sym...
| Main Authors: | , , , |
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| 格式: | 文件 |
| 语言: | English |
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Wolters Kluwer Medknow Publications
2021-01-01
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| 丛编: | Indian Pediatrics Case Reports |
| 主题: | |
| 在线阅读: | http://www.ipcares.org/article.asp?issn=2772-5170;year=2021;volume=1;issue=1;spage=57;epage=61;aulast=Kaur |