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Biology / Syndromes / Ion channels / Proteins / Long QT syndrome / Romano-Ward syndrome / KvLQT1 / KCNE1 / Jervell and Lange-Nielsen syndrome / Cardiac dysrhythmia / Health / Channelopathy


Genotype- and Phenotype-Guided Management of Congenital Long QT Syndrome John R.Giudicessi, BA, and Michael J. Ackerman, MD, PhD Abstract: Congenital long QT syndrome (LQTS) is a genetically heterogeneous group of herita
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Company

Phenotype-Guided Management / Mayo Medical Ventures / Genaissance Pharmaceuticals / Mayo Clinic Health Solutions / /

Country

United States / /

Currency

ATS / /

Event

Product Issues / FDA Phase / /

IndustryTerm

heterogeneous / /

MedicalCondition

rare multisystem disorders / heritable cardiac arrhythmia / Multisystem Long-QT Syndrome / lethal genetic disorder / sensorineural deafness / LQTS disease / torsades de pointes / periodic paralysis / recurrent cardiac arrest / simply ankyrin-B syndrome / syndactyly / sudden cardiac death / seizures / highly treatable genetic disorder / Congenital long QT syndrome / Andersen-Tawil syndrome / cardiac arrhythmias / sinus node dysfunction / bilateral sensorineural hearing loss / Timothy syndrome / cardiovascular disease / sick sinus syndrome / syncope / autism spectrum disorder / sudden cardiac arrest / atrioventricular block / deafness / SCD-predisposing cardiovascular disorders / heritable disorders / monogenic disorders / multisystem disorder / bradycardia / bilateral sensorineural deafness / congenital cardiac arrhythmia / hearing loss / disorders / long QT syndrome / /

MedicalTreatment

antibiotics / /

Organization

National Heart Lung and Blood Institute Ruth L. Kirschstein National Research Service / AR AD AD / /

Person

Melvin Scheinman / Ruth L. Kirschstein / John R.Giudicessi / Michael J. Ackerman / /

Position

Medical Scientist / Major / consultant / /

Product

triad / ketoconazole / erythromycin / thorazine / IK1 / KCNQ1 / IKs currents / LQT1 / JLN1 / KCNE2 / IKs / /

Technology

drug metabolism / Genotype / /

URL

http /

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