Lawhon S M, MacEwen G D, Bunnell W P
J Bone Joint Surg Am. 1986 Mar;68(3):424-9.
The cases of twenty-eight patients with the VATER association, which consists of various combinations of vertebral anomalies, anal atresia, tracheoesophageal fistula with esophageal atresia, radial dysplasia, and renal anomalies, were reviewed. Associated anomalies included deformities of the ribs and lower limbs, a two-artery umbilical cord, a congenital heart defect, and auricular deformities. Three children died in the first two years of life. Of the remaining twenty-five patients, twelve have required a total of seventeen orthopaedic procedures for the treatment of congenital scoliosis or deformity of the upper or lower extremities.
对28例患有VATER综合征的患者病例进行了回顾,该综合征包括脊柱异常、肛门闭锁、食管闭锁合并气管食管瘘、桡骨发育不良和肾脏异常的各种组合。相关异常包括肋骨和下肢畸形、双脐动脉、先天性心脏缺陷和耳部畸形。3名儿童在出生后的头两年内死亡。在其余25例患者中,12例因先天性脊柱侧凸或上肢或下肢畸形共需要进行17次骨科手术治疗。