Lange-Nielsen syndrome
Last reviewed 05/2021
The Lange-Nielsen syndrome is the association of QT prolongation with congenital deafness.
The inheritance is autosomal recessive.
The problems with cardiac arrhythmias may lead to sudden collapse.
You are currently on the
UK version of this site. To see content specific to your location,
please choose your country or region.
GPnotebook no longer supports Internet Explorer. To ensure the site functions as intended, please
upgrade your browser. Microsoft is encouraging users to upgrade to its more modern
Edge browser for improved security and functionality.