A case of congenital multiple epiphyseal dysplasia from the Late Migration Period graveyard in Drnholec (Czech Republic)

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Publikace nespadá pod Filozofickou fakultu, ale pod Lékařskou fakultu. Oficiální stránka publikace je na webu muni.cz.
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VARGOVÁ Lenka VYMAZALOVÁ Kateřina JAROŠOVÁ Ivana MAŘÍK Ivo HORÁČKOVÁ Ladislava TRAMPOTA František REBAY-SALISBURY Katharina RENDL Barbara KANZ Fabian ZLÁMALOVÁ Denisa

Rok publikování 2023
Druh Článek v odborném periodiku
Časopis / Zdroj International Journal of Paleopathology
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://www.sciencedirect.com/science/article/pii/S1879981722000584?via%3Dihub
Doi http://dx.doi.org/10.1016/j.ijpp.2022.11.003
Klíčová slova Congenital defects; Disproporcional growth; Skeletal dysplasia; Tooth cementum annulation (TCA); Langobards
Popis Objective To contribute to differential diagnosis of multiple epiphyseal dysplasia (MED) in archeological and clinical contexts. Materials A skeleton of a 30- to 45-year-old male (grave no. 806) from the Late Migration Period graveyard in Drnholec-Pod sýpkou (Czech Republic), radio-carbon dated to AD 492–530. Methods Morphological and metric analyses. Results Significant pathological changes were noted on ossa coxae and proximal ends of the femora, which appear similar to changes associated with Legg-Calvé-Perthes disease. X-ray examination made it possible to rule out pseudoachondroplasia, rickets and metabolic bone diseases. Conclusions The finding was evaluated as a probable case of congenital multiple epiphyseal dysplasia. Significance This case will contribute to the construction of estimates of the occurrence of this disease in historical populations and can be instructive for diagnostics in current medical practice. Limitations The final diagnosis is limited by the lack of genetic analysis. Suggestion for the future research Further clarification leading to diagnosis will benefit from genetic analysis and evaluation of skeletal remains throughout Europe.

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