Un posible caso de artrogriposis múltiple congénita
DOI:
https://doi.org/10.22201/iia.14055066p.2009.27208Keywords:
arthrogryphosis multiplex congenitalAbstract
One infant skeleton (number 145), showed a combination of abnormalities that are highly suggestive of arthrogryphosis multiplex congenital (amc). There are a very few reports in paleopathological literature about this kind of maladies, for that reason is necessary to describe and emit the possible diagnosis of amc, them could be used like comparative material. This case is part to modern-day popula-tion collection of human skeleton from the physical anthropology section from Department of Anatomy in Faculty of Medicina at Universidad Nacional Autónoma de México (Unam).
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http://creativecommons.org/licenses/by-nc-nd/4.0/