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Inherited knee disorders in the Medici family.

Identifieur interne : 000D06 ( Ncbi/Merge ); précédent : 000D05; suivant : 000D07

Inherited knee disorders in the Medici family.

Auteurs : Donatella Lippi [Italie] ; Marco Matucci-Cerinic [Italie] ; W R Alburyc [Australie] ; George M. Weisz [Australie]

Source :

RBID : pubmed:24439765

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English descriptors

Abstract

Reconstructing a medical condition which was existent centuries ago is limited by the lack of contemporaneous evidence-based descriptions in the accounts given by physicians and other observers. Despite these limitations modern paleopathological evidence, supplemented by techniques of historical investigation, have led to the conclusion that males in the Medici family typically suffered from a complex clinical entity with a triple pathology of stenotic spinal ankylosis, recurrent peripheral joint disease and erythematous skin disease; the Medici Syndrome. Examination of the knee joint is illustrative of recurrent joint disease both in the primary and secondary lines of the family. Pictorial and sculptural representations, if used cautiously, can assist in this retrospective process. The six cases presented here illustrate the involvement of the knee joint where the joint destruction ultimately led to an ankylosis.

DOI: 10.1016/j.knee.2013.11.006
PubMed: 24439765

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pubmed:24439765

Le document en format XML

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