Objective: The goal of this study was to analyze and differentially diagnose the presence of two large holes noted in the parietal bones of an individual and the presence of traumatic lesions.
Materials: A partially mummified young adult female associated with the Chinchorro culture, 4000 BP, from the coast of the Atacama Desert (northern Chile).
Methods: The bone lesions were evaluated macroscopically and radiologically. In addition, Sr isotopic analyses were performed on 62 individuals from eight sites associated with the Chinchorro culture.
Results: The parietal orifices are compatible with a rare anomaly of genetic origin known as foramina parietalia permagna (FPP). In addition, the cranial fracture pattern appear compatible with perimortem trauma, and Sr isotopes indicate a marine signal for Chinchorro populations.
Conclusions: This case serves as evidence that FPP was present in the early Andean populations and that endogamy and mutagenic factors might have contributed to its presence.
Significance: This paper expands our knowledge of the genetic anomalies that affected past populations and may contribute to our understanding of the etiologies of the condition.
Limitations: The absence of comparative FPP data inhibits comparative studies (with the exception of cases from California, USA).
Suggestions For Future Research: To explore in depth the genetic component of this condition in the Chinchorro populations.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.ijpp.2024.11.004 | DOI Listing |
Int J Paleopathol
December 2024
Field Museum of Natural History, Integrative Research Center, Chicago, USA; International Committee on Archaeological Heritage Management (ICAHM) Icomos, Chile. Electronic address:
Objective: The goal of this study was to analyze and differentially diagnose the presence of two large holes noted in the parietal bones of an individual and the presence of traumatic lesions.
Materials: A partially mummified young adult female associated with the Chinchorro culture, 4000 BP, from the coast of the Atacama Desert (northern Chile).
Methods: The bone lesions were evaluated macroscopically and radiologically.
Neuropediatrics
June 2024
Division of Neurology, Neurometabolics and Prevention, Department of Pediatrics, Goethe University Frankfurt, Frankfurt, Germany.
Foramina parietalia permagna (FPP) is a rare anatomical defect that affects the parietal bones of the human skull. FPP is characterized by symmetric perforations on either side of the skull, which are caused by insufficient ossification during embryogenesis. These openings are typically abnormally large and can range from a few millimeters to several centimeters in diameter.
View Article and Find Full Text PDFAn Pediatr (Engl Ed)
August 2021
Servicio de Pediatría y sus Áreas Específicas, Unidad de Neuropediatría, Hospital Clínico San Carlos, Madrid, Spain.
Childs Nerv Syst
May 2017
Department of Neurosurgery, Istanbul Bilim University, Sisli Florence Nightingale Hospital, Istanbul, Turkey.
Purpose: Foramina parietalia permagna is a variable intramembranous ossification defect of the parietal bones. Foramina parietalia permagna have an autosomal dominant inheritance, and it is showed that mutations in chromosome 5 and 11 are causing this anomaly. Enlarged parietal foramina occurs extremely rare.
View Article and Find Full Text PDFIntroduction: In forensic autopsy, pathologists are not particularly interested in the anatomical morphological variations of the skull bones, especially if those variations are not very frequent. Foramina parietalia permagna are developmental benign anomalies resulting from large ossification defects of the parietal bone.
Case Outline: Herein was presented a case of 80-year-old female, whose autopsy revealed congenital defect of parietal bones--enlarged parietal foramina.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!