Brugada Syndrome: Difference between revisions

Brugada Syndrome (view source)

500 bytes removed , 21 March 2013

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 {| class="wikitable" border="0" cellpadding="0" cellspacing="0" width="800px"
 |-
-!colspan="1"|'''Findings'''
+|- align=left
+!colspan="2"|'''Findings'''
 |- align=left
 |'''ECG'''
-|'''OMIM'''
+|'Type 1 ECG with coved type ST-elevation'
-|'''Gene'''
-|'''Protein'''
-|'''Functional role in cardiomyocytes'''
-|'''Effect of mutation'''
 |-
-!colspan="1"|'''And at least one of the following'''
+!colspan="2"|'''And at least one of the following'''
-|-
+|- align=left
-!colspan="1"|'''And at least one of the following'''
+|'''Clinical history'''
-|colspan="6" bgcolor="#FFFFCC"|'''OMIM:''' ''Online Mendelian Inheritance in Man'' compendium of human genes and genetic phenotypes; '''BrS1–BrS7:''' Brugada syndrome types 1–7; '''NC:''' no consensus; '''I<sub>Ca,L</sub>:''' L-type calcium current; '''I<sub>f</sub>:''' hyperpolarization-activated current; '''I<sub>K,ATP</sub>:''' ATP-sensitive potassium current; '''I<sub>Na</sub>:''' fast sodium current; '''I<sub>to</sub>:''' transient outward potassium current.
+|- Documented ventricular fibrillation
 |}