Foster H E, Cairns R A, Burnell R H, Malleson P N, Roberton D M, Tredwell S J, Petty R E, Cabral D A
Department of Pediatrics, British Columbia's Children's Hospital, Canada.
J Rheumatol. 1995 Mar;22(3):548-51.
We describe 2 HLA-B27 positive children with seronegative enthesopathy and arthropathy (SEA) syndrome who developed spontaneous (nontraumatic) atlantoaxial subluxation early in their disease course. Neither child had evidence of spinal cord compression but both had progressive atlantoaxial subluxation in spite of conservative treatment. Both underwent elective posterior cervical (C1-C2) fusion.
我们描述了2例患有血清阴性附着点病和关节病（SEA）综合征的HLA - B27阳性儿童，他们在疾病病程早期就出现了自发性（非创伤性）寰枢椎半脱位。两个孩子均无脊髓受压的证据，但尽管接受了保守治疗，两人均出现了进行性寰枢椎半脱位。两人均接受了选择性后路颈椎（C1 - C2）融合术。
