First Header Logo Second Header Logo

Jervell-Lange Nielsen Syndrome

"Jervell-Lange Nielsen Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

expand / collapse MeSH information
A form of long QT syndrome that is associated with congenital deafness. It is characterized by abnormal cardioelectrophysiology involving the VOLTAGE-GATED POTASSIUM CHANNEL. It results from mutation of KCNQ1 gene (Subtype 1 or JLN1) or the KCNE1 gene (Subtype 2 or JLN2).


expand / collapse publications
This graph shows the total number of publications written about "Jervell-Lange Nielsen Syndrome" by people in this website by year, and whether "Jervell-Lange Nielsen Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
_