Madelung’s deformity was first reported by Malgaigne in 1855, but the disorder is named for Madelung’s because of his detailed description, published in 1878. Classic Madelung’s deformity is believed to be hereditary, but a Madelung-type deformity can be caused by trauma to the distal radius physis, infection, isolated osteochondroma, or multiple hereditary exostosis. This rare condition usually presents between the ages of 6 and 13 years; girls are affected more frequently than boys (3:1). The deformity may go unnoticed for years, but with growth and the onset of puberty, pain, decreased range of motion, and cosmetic issues may manifest.1,2,3
Pathophysiology
- Madelung’s deformity is caused by abnormal growth arrest of the palmar-ulnar distal radius physis.3
- An abnormality of the palmar ligament that tethers the lunate to the palmar-ulnar radius epiphysis and metaphysis (Vickers ligament) is contributory.
- The disease process involves:
- Abnormal growth of the distal radial epiphysis and in many cases bowing of the radius.
- Arching of the radius
- Premature fusion of the ulnopalmar distal radial epiphysis.
- Delayed development of the ulnar and anterior parts of the distal radial epiphysis.
- Inclined radial distal joint surface to the anterior and ulnar area
- Anterior translation of the hand and the wrist
- Dorsal dislocation of the ulna in its distal posterior part
Related Anatomy
- Distal radius physis
- Palmar ligament
- Vicker’s ligament
- Lunate
- Ulna
Incidence and Related Conditions
- Madelung’s deformity is a rare disorder that frequently occurs bilaterally.
- The disease is linked with several skeletal disorders, including dyschondrosteosis, Turner syndrome, and Léri-Weill syndrome.
- Approximately 10% of children with fractures of the distal radius physis may experience growth arrest of the physis and subsequent deformity. Isolated distal radius deformity without radial shaft bowing is more commonly associated with trauma and repetitive trauma such as gymnastics. Madelung'sdeformity with a bowed forearm is more commonly associated with skeletal disorders like dyschondrosteosis.3
- The family history is often positive.
Differential Diagnosis
- Dyschondrosteosis
- Infection
- Inflammatory conditions (eg, rheumatoid arthritis)
- Léri-Weill syndrome
- Multiple hereditary exostosis
- Osteochondroma
- Rickets
- Trauma
- Turner syndrome