Abstract
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). © 2007 The Authors Journal compilation © 2007 Anatomical Society of Great Britain and Ireland.
Author supplied keywords
Cite
CITATION STYLE
Fernandes, T., & Costa, C. (2007). Klippel-Feil syndrome with other associated anomalies in a medieval Portuguese skeleton (13th-15th century). Journal of Anatomy, 211(5), 681–685. https://doi.org/10.1111/j.1469-7580.2007.00809.x
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.