Abstract
Study of a case of dyschondrosteosis (Léri-Weill syndrome) was detected in a sixth-century adult skeleton.
In addition to the typical characteristics of dyschondrosteosis (shortness of the forearms and lower legs accompanied by Madelung's deformity of the radius), examination of the skeleton revealed bilateral acetabular dysplasia.
No degenerative change (osteoarthrosis) was observed in the joints directly associated with these malformations.
Similar content being viewed by others
References
Brocher, J.E.W., Klein, D.: Die Dyschondrosteose. Fortschr. Geb. Roentgenstr Nuklearmed 96, 496 (1962)
Jeune, M., Larbre, F.: Un cas de dyschondrostéose. Pédiatrie. 9, 58 (1954)
Kaufmann, H., Lagier, R., Baud, C.A.: Un cas de nanisme par dyschondrostéose au VIe siècle à Genève. Actes du XIIIe Colloque des anthropologistes de langue française. Caen 1977 (in press)
Langer, L.O.: Dyschondrosteosis, a hereditable bone dysplasia with characteristic roentgenographic features. Am. J. Roentgenol. Radium Ther. Nucl. Med. 45, 178 (1965)
Léri, A., Weill, J.: Une affection congénitale et symétrique du développement osseux: la dyschondrostéose. Bull. Soc. Méd Hôpitaux Paris 45, 1491 (1929)
Oikawa, K. et al.: Dyschondrosteosis associated with endocrine dysfunctions and mental deficiency. Tohoku J. Exp. Med. 114, 287 (1974)
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Lagier, R., Kaufmann, H. & Baud, C.A. Dyschondrosteosis (Léri-Weill Syndrome) observed in a VIth century skeleton. Skeletal Radiol. 3, 102–104 (1978). https://doi.org/10.1007/BF00363962
Issue Date:
DOI: https://doi.org/10.1007/BF00363962