Differential diagnosis of metabolic disease in a commingled sample from 19th century Hisban, Jordan

This research attempts a differential diagnosis of skeletal lesions in a commingled sample from Hisban, Jordan, focusing on non-adults in the assemblage. 2,883 well-preserved skeletal elements and 9 relatively complete skulls representing an MNI of 32 non-adults (<18 years old). All skeletal elem...

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Bibliographic Details
Published inInternational journal of paleopathology Vol. 33; pp. 220 - 233
Main Authors Perry, Megan A., Edwards, Emily
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Inc 01.06.2021
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Summary:This research attempts a differential diagnosis of skeletal lesions in a commingled sample from Hisban, Jordan, focusing on non-adults in the assemblage. 2,883 well-preserved skeletal elements and 9 relatively complete skulls representing an MNI of 32 non-adults (<18 years old). All skeletal elements were observed macroscopically and pathophysiological processes underlying any lesions or other anomalies were assessed, followed by a comparative approach to rule out potential diagnoses. The skeletal lesions observed were caused by inflammation due to chronic hemorrhaging, marrow hyperplasia due to an increase in hemopoiesis, rapid bone growth, and the impact of biomechanical strain on poorly mineralized elements. Rickets, scurvy, and acquired anemias best fit this pattern of lesions, although inflammation from other sources such as trauma or infection could not be definitively ruled out. The in utero and postnatal environments at Hisban were conducive to the development of vitamin C and D deficiencies from birth until 2 years of age. The analysis of commingled remains requires an ontological shift in the importance of the individual to the population in paleopathology. This investigation demonstrates the efficacy of a combined biological and comparative approach in differential diagnosis in complicated commingled collections. In addition, it emphasizes the importance of the mother-infant dyad in understanding metabolic disease. Histological and radiographic analyses were not included in this diagnostic study due to COVID-19 travel restrictions. Isotopic analysis to investigate childhood diet and histological and radiographic analyses to assess survival of deficiencies.
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ISSN:1879-9817
1879-9825
DOI:10.1016/j.ijpp.2021.05.003