Long QT syndrome: Difference between revisions
Jump to navigation
Jump to search
imported>Robert Badgett (New page: {{subpages}} '''Long QT syndrome''' is "condition that is characterized by episodes of fainting (syncope) and varying degree of ventricular arrhythmia as indicated by the prolonged...) |
imported>Robert Badgett mNo edit summary |
||
| Line 1: | Line 1: | ||
{{subpages}} | {{subpages}} | ||
'''Long QT syndrome''' is "condition that is characterized by episodes of fainting ([[syncope]]) and varying degree of ventricular [[arrhythmia]] as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Romano-Ward Sydrome and Jervell-Lange Nielsen Syndrome.<ref>{{MeSH}}</ref><ref name="pmid18184962">{{cite journal |author=Roden DM |title=Clinical practice. Long-QT syndrome |journal=N. Engl. J. Med. |volume=358 |issue=2 |pages=169–76 |year=2008 |pmid=18184962 |doi=10.1056/NEJMcp0706513|url=http://content.nejm.org/cgi/content/full/358/2/169}}</ref> | '''Long QT syndrome''' is "condition that is characterized by episodes of fainting ([[syncope]]) and varying degree of ventricular [[arrhythmia]] as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Romano-Ward Sydrome and Jervell-Lange Nielsen Syndrome."<ref>{{MeSH}}</ref><ref name="pmid18184962">{{cite journal |author=Roden DM |title=Clinical practice. Long-QT syndrome |journal=N. Engl. J. Med. |volume=358 |issue=2 |pages=169–76 |year=2008 |pmid=18184962 |doi=10.1056/NEJMcp0706513|url=http://content.nejm.org/cgi/content/full/358/2/169}}</ref> | ||
==References== | ==References== | ||
<references/> | <references/> | ||
Revision as of 13:52, 31 January 2008
Long QT syndrome is "condition that is characterized by episodes of fainting (syncope) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Romano-Ward Sydrome and Jervell-Lange Nielsen Syndrome."[1][2]
References
- ↑ Anonymous (2024), Long QT syndrome (English). Medical Subject Headings. U.S. National Library of Medicine.
- ↑ Roden DM (2008). "Clinical practice. Long-QT syndrome". N. Engl. J. Med. 358 (2): 169–76. DOI:10.1056/NEJMcp0706513. PMID 18184962. Research Blogging.