D2I2.
genetic

Jervell and Lange-Nielsen syndrome

Jervell and Lange-Nielsen (JLNS) is a rare type of long QT syndrome associated with severe, sensorineural hearing loss. Those with JLNS are at risk of abnormal heart rhythms called arrhythmias, which can lead to fainting, , or sudden death. JLNS, like other forms of long QT syndrome, causes the muscle to take longer than usual to recharge between beats. It is caused by responsible for producing ion channels that carry transport out of cells. The condition is usually diagnosed using an , but genetic testing can also be used. Treatment includes lifestyle measures, beta , and implantation of a defibrillator in some cases. It was first described by Anton Jervell and Fred Lange-Nielsen in 1957.

Underlined words are explained — tap any of them.

Symptoms — what it feels like

  • ·Blackouts, , sensorineural deafness

Causes — why it happens

  • ·

Treatment

  • ·Beta , implantable cardioverter defibrillator

Complications

  • ·Sudden death
Plain-language summary adapted from Wikipedia. Not medical advice.