Eber S W, Luhr H G, Spoerri O, Weigel W, Westmeier M
Z Kinderchir. 1986 Oct;41(5):263-6. doi: 10.1055/s-2008-1043355.
The possibility of plastic surgery in acrocephalosyndactylia syndrome during infancy is shown. Due to her main signs and symptoms and the mode of inheritance the patient suffered from an acrocephalosyndactylia syndrome type III (Saethre-Chotzen). Craniofacial surgery with frontal craniotomy, turn of frontal bone and frontal orbital advancement were performed at the age of eight months, using bone plates developed by Luhr. The reconstruction gave an aesthetically satisfactory result, and further development was normal. The condition for a good result is the cooperation between plastic surgeons, neurosurgeons, anaesthesiologists and paediatricians in specialised centres.
本文展示了在婴儿期进行尖头并指综合征整形手术的可能性。根据患者的主要体征和症状以及遗传方式，诊断其患有III型尖头并指综合征（塞特雷-乔岑综合征）。患儿8个月大时，采用鲁尔研发的骨板进行了颅面手术，包括额部开颅、额骨翻转和额眶前移。手术重建取得了令人满意的美学效果，且患儿后续发育正常。取得良好效果的条件是专业中心的整形外科医生、神经外科医生、麻醉医生和儿科医生之间的合作。
