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Skeletal dysplasia of an adult male from medieval Łekno in Poland, Central Europe

Bibliographic Data

ID12371021
AuthorsMagdalena D Matczak (0000-0003-2934-0036, Department of Archaeology, Classics, and Egyptology University of Liverpool Liverpool UK, corresponding author), Marta Krenz‐niedbała (0000-0001-7420-5621, Institute of Human Biology and Evolution, Faculty of Biology Adam Mickiewicz University in Poznań Poznań Poland), Sylwia Łukasik (0000-0003-2210-7434, Institute of Human Biology and Evolution, Faculty of Biology Adam Mickiewicz University in Poznań Poznań Poland), J E Buikstra (0000-0003-0206-0165, Center for Bioarchaeological Research Arizona State University Tempe Arizona USA), Andrzej Marek Wyrwa (0000-0002-4370-6877, Faculty of History Adam Mickiewicz University in Poznań Poznań Poland), J Pearson (0000-0001-6503-1041, Department of Archaeology, Classics, and Egyptology University of Liverpool Liverpool UK)
Year2022
Volume32
Issue6
Pages1300-1309
Publication date2022-08-17
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueInternational Journal of Osteoarchaeology (JOURNAL)
Journal identifiersISSN: 1047-482X • E-ISSN: 1099-1212
PublisherWiley (PUBLISHER • GB)
DOI10.1002/oa.3155
OpenAlexW4292295384
LanguageEN
Citations received2
References cited23

The skeletal dysplasias are a group of more than 450 heritable disorders that affect bone and cartilage, along with muscles, tendons, and ligaments. Achondroplasia is one of the most common skeletal dysplasias in both current and past populations. It can be transmitted intergenerationally, or it can result from a mutation. This paper aims to describe the lesions visible on the skeleton of a 30–45 year old male with achondroplasia, who lived during the 9th–11th centuries AD (medieval period) in Łekno, Poland. The Łekno settlement complex (Site 3) includes a cemetery with approximately 400 burials of monks and local lay people. Macroscopic examination facilitated a differential diagnosis that identified a probable case of achondroplastic dwarfism, combined with Léri–Weill dyschondrosteosis and ulnar hemimelia. This is the first case of dwarfism in the bioarchaeological literature that had been documented and visualized using 3D modelings, which were used to show quantitative differences in articular surface areas between the achondroplastic individual and contemporaries of normal stature. Ulnar hemimelia is most commonly seen today as a component of skeletal dysplasias. The right ulna of this male was significantly shorter than the right radius and the left ulna. It is probable that he had multiple skeletal dysplasia (achondroplasia, Léri–Weill dyschondrosteosis) as well as ulnar hemimelia as a component of achondroplasia. The combination of these disorders has not been previously reported in the bioarchaeological literature, and this individual is also the first case of achondroplasia and Léri–Weill dyschondrosteosis from the medieval period in Central Europe. As such, this example is used here to provide insights on a variety of different diseases, syndromes, and conditions in Polish medieval populations and that will help in future identification of rare diseases from archaeological sites

Achondroplasia · Biology · Dwarfism · Dysplasia · Ossification · Osteochondrodysplasia · Pathology · Skeleton (computer programming · Ulna · Forensic Anthropology and Bioarchaeology Studies · Genital Health and Disease · Medical and Biological Sciences · Medicine · Anatomy · Genetics · Surgery

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Unique citing works2
Citations per year0,67
Citation span2023 - 2024 (2)
Citation velocityrecent
Highly citedNo
Citation typesNeutral: 2
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