Long QT Syndrome is considered a rare disease as according to literature it affects around 1-2000 people. Long QT syndrome is usually inherited in an autosomal dominant manner. This means that a child has a 50% chance of inheriting the condition if one parent carries the gene mutation responsible for Long QT . There are also autosomal recessive forms, where a child must inherit the gene mutation from both parents to develop the condition (Jervell and Lange-Nielsen syndrome).
Some experts think Long QT Syndrome is probably more common than the stats show. This is due to improved awareness in the medical community, improved diagnostic techniques, and the recognition of milder or asymptomatic cases.