Fernandes Teresa, Costa Catarina
Laboratório de Antropologia Biológica, Departamento de Biologia, Universidade de Evora, Portugal.
J Anat. 2007 Nov;211(5):681-5. doi: 10.1111/j.1469-7580.2007.00809.x. Epub 2007 Sep 7.
Klippel-Feil syndrome, or synostosis of the cervical spine, is the result of an abnormal division of somites during embryonic development. This report analyses an adult male (exhumed from a Portuguese graveyard dating from the 13th to the 15th century) with malformations in the cranium and vertebral column. Besides the lesions that are typical of Klippel-Feil syndrome type II, other defects usually linked to this pathology are described (occipito-atlantal fusion, hemivertebrae, butterfly vertebrae, cervical rib, changes in normal number of vertebral segments and a possible Sprengel deformity).
克-费综合征,即颈椎融合畸形,是胚胎发育过程中体节异常分化的结果。本报告分析了一名成年男性(从13至15世纪的葡萄牙墓地挖掘出土),其颅骨和脊柱存在畸形。除了典型的II型克-费综合征病变外,还描述了通常与该病症相关的其他缺陷(枕寰融合、半椎体、蝴蝶椎、颈肋、椎体节段数量异常以及可能存在的先天性高肩胛畸形)。