Tags: Disease.
Legius syndrome (LS) is an autosomal dominant condition characterized by cafe au lait spots. It was first described in 2007 and is often mistaken for Neurofibromatosis type I (NF-1). It is caused by mutations in the SPRED1 gene. It is also known as Neurofibromatosis Type 1-like syndrome (NFLS).The syndrome is named after Eric Legius Professor at the KU Leuven. It is a RASopathy.