Unclassified sudden infant death due to congenital long QT syndrome with TRPM4 mutation

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...

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Bibliographic Details
Main Authors: Jasleen Kaur, Ratna Dua Puri, Sharmila B Mukherjee, Bijal Vyas
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2021-01-01
Series:Indian Pediatrics Case Reports
Subjects:
apnea
channelopathy
corrected qt
schwartz score
Online Access:http://www.ipcares.org/article.asp?issn=2772-5170;year=2021;volume=1;issue=1;spage=57;epage=61;aulast=Kaur

Internet

http://www.ipcares.org/article.asp?issn=2772-5170;year=2021;volume=1;issue=1;spage=57;epage=61;aulast=Kaur

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