Long qt syndrome type 5--what are the treatments?

AICD. Type 5 lqt is due to decrease function of the potassium channel involved in the generation of the slow potassium current . It is uncommon present in 1% of the total cases of lqt . This involve mutation of the protein called mink in the beta subunit of the potassium channel there is no treatment other than a cardiodefibriilator.

Related Questions

My 19yo daughter has been diagnosed with long qt syndrome. What treatments are possible?

Long QT interval. Beta blockers such as Inderal (propranolol) are usually the first line of treatment. Read more...
Long qt. Medication is a must, in some you need defibrillator or sympathectomy, depends..I am an expert in the field. You can consult me or one of us if you need more detailed info. www.healthtap.com/volkantuzcu. Read more...

What is the definition or description of: long qt syndrome?

Sudden death... Romano-ward, without congenital deafness and jervell-lange-nielsen, with deafness. Both refer to a delay in the repolarization time of the cardiac cycle, when there is a "vulnerable" period. The time between the q wave and the t wave. A premature beat, which are common, in this period can cause deadly arrhythmias, like torsades de pointes. Tdp occurs when heart rate increases, consult cardiolog. Read more...

How likely is long qt syndrome to kill me?

Not super likely. Long qt syndrome (lqts) is a congenital heart defect that may result in syncope and lead to sudden cardiac death, which usually occurs in otherwise healthy young individuals. Lqts is thought to cause about 4000 deaths in the United States each year. The chance of someone dying from this is approximately 6% by the age of 40 years. (from medscape's emedicine). Read more...
Unlikely but. You should have regular cardiology follow up and follow all recommended precautions. Read more...
Long qt . Depends on the type of genetic defect you have and several other factors such as the degree of QT lengthening on your ECG . Read more...