| Literature DB >> 17850283 |
Teresa Fernandes1, Catarina Costa.
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).Entities:
Mesh:
Year: 2007 PMID: 17850283 PMCID: PMC2375781 DOI: 10.1111/j.1469-7580.2007.00809.x
Source DB: PubMed Journal: J Anat ISSN: 0021-8782 Impact factor: 2.610