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Article

Genetic variants for long QT syndrome among infants and children from a statewide newborn hearing screening program cohort.

The Journal of pediatrics - 1 Mar 2014

Chang Ruey-Kang R, Lan Yueh-Tze, Silka Michael J, Morrow Hallie, Kwong Alan, Smith-Lang Janna, Wallerstein Robert, Lin Henry J

Abstract excerpt

OBJECTIVES: Autosomal recessive long QT syndrome (LQTS), or Jervell and Lange-Nielsen syndrome (JLNS), can be associated with sensorineural hearing loss. We aimed to explore newborn hearing screening combined with electrocardiograms (ECGs) for early JLNS detection. STUDY DESIGN: In California, we conducted statewide, prospective ECG screening of children ≤ 6 years of age with unilateral or bilateral, severe or...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 24388587
DOI: 10.1016/j.jpeds.2013.11.011
PMCID: PMC3943925

Genes

KCNQ1

Variants

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