Gordon's Syndrome is described as an autosomal dominant condition with the
characteristics of short stature, a stiff spine, camptodactyly (89%), cleft
palate (27%) and club feet (73%). The authors present a case report of a p
atient with this rare entity complicated by an unusual complex spinal defor
mity. There are no prior reports in the literature concerning operative or
nonoperative management of deformity in this patient population. Scoliosis
in Gordon's Syndrome shares the characteristics of an arthrogrypotic neurom
uscular curve and demands extensive soft tissue release for optimal correct
ion.