" /> Larsen syndrome - CISMeF





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.;

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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.

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28/07/2025


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