eMedicine Specialties > Orthopedic Surgery > Pediatrics
Madelung Deformity: Follow-up
Updated: Mar 4, 2008
Outcome and Prognosis
Goals for surgical correction of MD consist primarily of pain relief and correction of the cosmetic deformity. A secondary goal is to increase range of motion. Most patients who undergo biplane osteotomy with ulnar length adjustment or the crescentic radial osteotomy of Carter and Ezaki19 attain both primary goals. Range of motion usually is only moderately improved at best. It should be noted that pain relief can be substantial and can be achieved quickly following release of the volar Vickers ligament.
Future and Controversies
Genetic links of MD to the SHOX gene on the X chromosome are emerging. No simple Mendelian inheritance pattern exists, so more than one gene most likely is involved. The interaction of the SHOX locus with other genes and transcription factors is not known and will be an area of future research. Results may provide a more complete answer to the link between dyschondrosteosis and MD.
Historically, surgical treatment of MD has been a closing wedge biplane osteotomy in conjunction with an ulnar shortening osteotomy of the distal ulna. Recently, a new procedure that addresses the deformity with a dome-shaped osteotomy, a release of Vickers ligament, and a reduction of the DRUJ without an ulnar procedure has been successfully used. This procedure shows great promise.
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Follow-up: Madelung Deformity |
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References
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Further Reading
Keywords
progressive subluxation of the wrist, idiopathic curvature of the radius, MD, wrist pain, wrist deformity, spontaneous forward subluxation of the hand, Leri-Weill dyschondrosteosis, multiple hereditary osteochondromatosis, Ollier disease, achondroplasia, multiple epiphysial dysplasia, mucopolysaccharidoses, mucopolysaccharidosis, Hurler syndrome, Morquio syndrome
Follow-up: Madelung Deformity