Preferred Label : Larsen syndrome;
ICD-11 definition : Larsen syndrome is a rare genetic disorder characterized 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.;
Origin ID : 607849551;
Automatic exact mappings (from CISMeF team)
Larsen syndrome is a rare genetic disorder characterized 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.
