The Klippel-Feil Syndrome (KFS) is a rare complex congenital condition resulting from a failure in normal segmentation during the development of an embryo’s mesodermal somites, between the third and eighth week of gestation, characterized by the fusion of the cervical vertebrae
Elena Varotto, M.M. (2020). Klippel-Feil Syndrome in an ancient Sardinian population (16th century AD) – A paleopathological study of four cases from the San Michele cemetery in Alghero. In G. Spani, E. Varotto (a cura di), Malattie e medicina tra letteratura, storia e antropologia (pp. 139-153). Holden : Quod Manet.
Klippel-Feil Syndrome in an ancient Sardinian population (16th century AD) – A paleopathological study of four cases from the San Michele cemetery in Alghero
Elena Varotto
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;
2020-01-01
Abstract
The Klippel-Feil Syndrome (KFS) is a rare complex congenital condition resulting from a failure in normal segmentation during the development of an embryo’s mesodermal somites, between the third and eighth week of gestation, characterized by the fusion of the cervical vertebrae
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