Catalog

Larsen syndrome

No MMS code

Link to WHO Definition

Larsen syndrome – http://id.who.int/icd/entity/607849551

Larsen syndrome is a rare genetic disorder characterised by congenital dislocation of numerous joints, joint hypermobility and distinctive facial features (flat nasal bridge, hypertelorism and occasionally cleft palate). Respiratory problems due to lack of rigidity of the upper airways may occur.