کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
9960132 1577538 2005 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Developmental Aspects of Long QT Syndrome Type 3 and Brugada Syndrome on the Basis of a Single SCN5AMutation in Childhood
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی کاردیولوژی و پزشکی قلب و عروق
پیش نمایش صفحه اول مقاله
Developmental Aspects of Long QT Syndrome Type 3 and Brugada Syndrome on the Basis of a Single SCN5AMutation in Childhood
چکیده انگلیسی
We conclude that electrocardiographic characteristics of LQT3 and BS show age-dependent penetrance. A QT prolongation and conduction disease were present from birth onwards, whereas ST-segment elevation only developed >5 years. Good tools for clinical diagnosis of LQT3 in this family are QTcat the lowest HR and ΔQT after a pause in a Holter, even at very young age.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of the American College of Cardiology - Volume 46, Issue 2, 19 July 2005, Pages 331-337
نویسندگان
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