Jervell-Lange Nielsen Syndrome

Known as: Jervell And Lange-Nielsen Syndrome 1, Cardio-Auditory-Syncope Syndrome, Jervell and Lange Nielsen Syndrome 
A form of long QT syndrome that is associated with congenital deafness. It is characterized by abnormal cardioelectrophysiology involving the VOLTAGE… (More)
National Institutes of Health

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Autosomal recessive inheritanceCardiovascular systemChestCongenital sensorineural hearing loss
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JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder)

Papers overview

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Highly Cited
2011
Highly Cited
2011
2011 ACCF/AHA/SCAI Guideline for Percutaneous Coronary Intervention. A report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines and the…
published online Nov 7, 2011; J. Am. Coll. Cardiol. Mukherjee, Brahmajee K. Nallamothu, and Henry H. Ting Richard A. Lange, Laura… (More)
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Highly Cited
2008
Highly Cited
2008
Accurate Multiplex Polony Sequencing of an Evolved Bacterial Genome
June 2005). 4. R. M. Alexander, J. Exp. Biol. 160, 55 (1991). 5. G. A. Cavagna, N. C. Heglund, C. R. Taylor, Am. J. Physiol. 233… (More)
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2006
2006
Clinical course and risk stratification of patients affected with the Jervell and Lange-Nielsen syndrome.
INTRODUCTION Data regarding risk factors and clinical course of patients affected with Jervell and Lange-Nielsen syndrome (JLNS… (More)
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2006
2006
Jervell-Lange Nielsen syndrome in a family with the long QT Syndrome (LQTS).
A child with Jervell-Lange Nielsen syndrome is presented from Kolkata. Family study showed that the other family members are… (More)
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2002
2002
Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome.
Jervell and Lange-Nielsen syndrome (JLNS) is characterized by sensorineural deafness, QT prolongation, abnormal T waves… (More)
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Highly Cited
2000
Highly Cited
2000
A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly.
The LQT1 locus (KCNQ1) has been correlated with the most common form of inherited long QT (LQT) syndrome. LQT patients suffer… (More)
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2000
2000
Cochlear implantation in Jervell and Lange-Nielsen syndrome.
Jervell and Lange-Nielsen syndrome represents a rare, autosomal recessive cause of congenital deafness. Affected patients have a… (More)
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Highly Cited
1997
Highly Cited
1997
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.
The Jervell and Lange-Nielsen syndrome (JLNS) comprises profound congenital sensorineural deafness associated with syncopal… (More)
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1997
1997
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous
Jervell Lange-Nielsen syndrome (JLNS) is a recessive disorder with congenital deafness and long-QT syndrome (LQTS). Mutations in… (More)
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Highly Cited
1997
Highly Cited
1997
KCNE1 mutations cause Jervell and Lange-Nielsen syndrome
 
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