Marfan syndrome
Marfan syndrome is an autosomal dominant disorder affecting connective tissue, caused by an abnormal production of the protein fibrillin-1, caused by a mutation in the FBN1 gene located on chromosome 15. This condition causes alterations in the eyes, bones, heart, blood vessels, lungs, and central nervous system.
We use modern and excellent surgical techniques to intervene on the pathology “Marfan syndrome“
From an orthopedic point of view, Marfan syndrome may include:
- excessive bone growth (long limbs and fingers)
- hyperlaxity of the ligaments: genu recurvatum
- scoliosis and kyphosis
- flat feet
- chest deformity: pectus excavatum or curatum