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Objectives: The aim of this work is to study age, sex, and population variations in epiphyseal fusion and persistence of the epiphyseal line in the appendicular skeleton of two identified modern (19th-20th c.) adult skeletal samples, using a specifically designed macroscopic scoring method. The use of epiphyseal closure and persistence of the epiphyseal line as an adult-age marker is also discussed.
Materials And Methods: This study examined 981 adult skeletons of both sexes from two identified modern (20th c.) skeletal samples from the Sassari Collection (Museum of Anthropology, University of Bologna, Italy) and the Colecção de Esqueletos Identificados (Museum of Anthropology, University of Coimbra, Portugal). Our scoring method considers a five-degree scale, from nonfusion (Degree 0) to complete fusion (Degree 4). In addition, the persistence of the epiphyseal line, a feature that is not commonly collected during routine anthropological analyses, is taken into account here as Degree 3.
Results: Intra- and interobserver errors of 1.2% and 5.2%, respectively, were found, suggesting a good reproducibility of this scoring method. Some sites show variable degrees of epiphyseal fusion still in adult skeletons (e.g., secondary center of ossification of the clavicle, iliac crest, ischial tuberosity, distal epiphysis of the radius and ulna).
Conclusions: Population differences have been observed, showing a delay in the complete epiphyseal closure for the Sassari sample compared to the Coimbra sample. Degree 3 seems to be a good adult-age indicator for individuals less than 35-year-old.
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http://dx.doi.org/10.1002/ajpa.23839 | DOI Listing |
Clin Case Rep
September 2025
Department of Pediatrics Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan Hubei China.
Brachyolmia type 4 (BCYM4, OMIM 612847) is a rare skeletal dysplasia characterized by mild epiphyseal and metaphyseal abnormalities. We report a Chinese boy with brachyolmia caused by a novel compound heterozygous mutation in the gene. Prenatal ultrasound revealed shortened long bones, and his birth length was markedly reduced (45 cm, -3.
View Article and Find Full Text PDFJ Clin Med
August 2025
Department of Morpho-Functional Sciences I, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.
: The epiphyseal vascularization of long bones generates a particular flow pattern that is important for adequate angiogenesis to be achieved. Imaging reveals that vessel development in murine long bone involves the expansion and anastomotic fusion of endothelial buds. Impaired blood flow leads to defective angiogenesis and osteogenesis and downregulation of Notch signaling in endothelial cells.
View Article and Find Full Text PDFBiomaterials
August 2025
Pediatric Orthopaedic Hospital, Honghui Hospital, Xi'an Jiaotong University, Xi'an, 710054, China; Xi'an Key Laboratory of Skeletal Developmental Deformity and Injury Repair, Xi'an, 710054, China; Research Center for Skeletal Developmental Deformity and Injury Repair, School of Life Science and Medi
Epiphysis is an organized and dynamically evolving developmental tissue that is susceptible to physical damage. At present, significant challenges in developing complex and controllable substitutes for epiphyses persist. In this study, human bone marrow mesenchymal stem cell (hBMSC) microspheres and recombinant human Indian hedgehog (IHH) were used to simulate the key mechanisms of bone development: mesenchymal condensation and biochemical signaling.
View Article and Find Full Text PDFCureus
July 2025
Department of Family Medicine, Demiroglu Science University, Istanbul, TUR.
This case report describes a complex diagnostic challenge in a 10-year-old male presenting with persistent and progressively worsening hip pain. The initial clinical suspicion centered on slipped capital femoral epiphysis (SCFE), a common orthopedic condition in adolescents often associated with obesity and characterized by displacement of the femoral head at the growth plate. Standard radiographs suggested potential epiphyseal abnormalities, raising concerns for SCFE.
View Article and Find Full Text PDFAnn Plast Surg
July 2025
From the Division of Plastic and Reconstructive Surgery, Department of Surgery, Weill Cornell Medicine/New York-Presbyterian Hospital, New York, NY.
Vascularized fibular epiphyseal transfer (VFET) has emerged as a reconstructive option for pediatric patients requiring limb salvage with preservation of growth potential. We presented 2 cases of VFET to the humerus following oncologic resection for osteosarcoma in children aged 11 and 5 years. Both cases demonstrated growth plate viability postoperatively, with serial imaging confirming annual growth rates of 0.
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