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We Only Find What We Look For: Fetal Heart Rate and the Diagnosis of Long QT Syndrome

Long QT syndrome (LQTS), an inherited channelopathy, is a common cause of arrhythmic death in infants, children and young adults. Although many LQTS genes have been identified, most (~75%) of LQTS mutations are found in KCNQ1, KCNH2 or SCN5A. In most cases, treatment for LQTS is successful and modif...

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Bibliografske podrobnosti
izdano v:Circ Arrhythm Electrophysiol
Main Authors: Cuneo, Bettina F., Strasburger, Janette F.
Format: Artigo
Jezik:Inglês
Izdano: 2015
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4552049/
https://ncbi.nlm.nih.gov/pubmed/26286300
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCEP.115.003196
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