Marfan Syndrome Research Today is a free monthly online journal that collates and summarizes the latest research about Marfan Syndrome, including details on genetics, causes, symptoms, treatment.

Infantile scoliosis in Beals syndrome: the use of a non-fusion technique for surgical correction.

Martin AG, Foguet PR, Marks DS, Thompson AG, Child AH

Royal Orthopaedic Hospital, Spinal Surgery, Birmingham, UK, antmartinincardiff@hotmail.com.

Beals syndrome (congenital contractural arachnodactyl) is a genetic disorder of the connective tissue phenotypically related to Marfan syndrome. It is characterised by dolichostenomelia, arachnodactyly, multiple joint contractures, crumpled ears, hypoplastic muscles and scoliosis. The latter, the most important clinical feature of this rare condition, presents in the infantile and juvenile age group and has a tendency to rapid progression. Bracing often fails to control the scoliosis and surgery is the recommended treatment. We present our experience of two cases managed with the paediatric Isola instrumentation and a non-fusion technique.

Published 5 April 2006 in Eur Spine J, 15(4): 433-9.
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