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...
| المؤلفون الرئيسيون: | , , , |
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| التنسيق: | مقال |
| اللغة: | English |
| منشور في: |
Wolters Kluwer Medknow Publications
2021-01-01
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| سلاسل: | Indian Pediatrics Case Reports |
| الموضوعات: | |
| الوصول للمادة أونلاين: | http://www.ipcares.org/article.asp?issn=2772-5170;year=2021;volume=1;issue=1;spage=57;epage=61;aulast=Kaur |