Results 71 to 80 of about 16,830 (226)

Assessing the Impact of Wear on the Recordability of Linear Enamel Hypoplasia: A Quantitative Approach

American Journal of Biological Anthropology, Volume 188, Issue 3, November 2025.
ABSTRACT Objectives This study proposes a standardized, empirically grounded framework for assessing the recordability of linear enamel hypoplasia (LEH) in archeological dental samples. Despite the frequent use of LEH as a skeletal stress indicator, there is no consensus on whether and how to account for dental wear in recording protocols.
Sacha Kacki, IJk van Hattum, Caroline Laforest, Caroline Polet, Frédéric Santos, Sarah Schrader, Sébastien Villotte   +6 more
wiley   +1 more source

Thoracic spondylolisthesis and spinal cord compression in diffuse idiopathic skeletal hyperostosis: a case report

Journal of Medical Case Reports, 2017
Background Diffuse idiopathic skeletal hyperostosis has long been regarded as a benign asymptomatic clinical entity with an innocuous clinical course. Neurological complications are rare in diffuse idiopathic skeletal hyperostosis.
Yasutaka Takagi, Hiroshi Yamada, Hidehumi Ebara, Hiroyuki Hayashi, Takeshi Iwanaga, Kengo Shimozaki, Yoshiyuki Kitano, Kenji Kagechika, Hiroyuki Tsuchiya   +8 more
doaj   +1 more source

Porotic Hyperostosis in the Eastern Mediterranean [PDF]

, 1978
Porotic hyperostosis is bone expansion caused by hypertrophy of blood-forming marrow. It usually affects the skull diploë in adults and the long bones, face, skull vault, and sometimes the trunk in children, often with some thinning and porosity in the ...
Angel, J. Lawrence
core   +1 more source

Melorheostosis: Clinical, radiological, and histopathological features with a literature review

Physiological Reports, Volume 13, Issue 21, November 2025.
Abstract Melorheostosis is a rare sclerosing bone dysplasia that can clinically and radiologically mimic common bone disorders, particularly in atypical presentations. Its heterogeneous manifestations and limited awareness among clinicians frequently contribute to diagnostic delays or misdiagnosis. We report the case of a 34‐year‐old woman with chronic
Elif Koca, Şeyhmus Kavak, Bilal Demir, Nil Comunoglu, Fatih Kantarci, Oguzhan Koca   +5 more
wiley   +1 more source

Infantile Cortical Hyperostosis

Annals of Surgery, 1957
THE syndrome that has become known as infantile cortical hyperostosis, after the suggestion of Caffey and Silverman,1 is characterized by the usually sudden onset of swelling of the face, thorax or extremities, hyperirritability, fever, fluctuating course and roentgenographic evidence of periosteal new-bone formation.
S J, O'CONNOR, J C, IVANOFF
openaire   +5 more sources

JAK Inhibitors for Treatment of SAPHO Syndrome: A Systematic Review of 72 Cases

ACR Open Rheumatology, Volume 7, Issue 10, October 2025.
Objective Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome usually involves bones, joints, and skin. Due to a lack of known pathogenesis and clinical trials, there is no standard treatment of SAPHO syndrome. Because none of the current treatments have a high efficacy and the risk of relapse is high, new treatment options for ...
Patrick Fazeli, Saeed Bahramian, Kimia Farahmand, Hamed Ghoshouni, Yalda Farahmand, Amirali Soheili, Leyla Bagheri, Huria Memari, Aydin Feyzi, Seyed Mohammad Vahabi   +9 more
wiley   +1 more source

A Framework for Anemia Differential Diagnosis in Paleopathology Incorporating Metric Methods

American Journal of Biological Anthropology, Volume 188, Issue 1, September 2025.
ABSTRACT Objectives This paper explores metric manifestations of anemia in crania undergoing growth and development using micro‐CT imaging. It proposes a framework for assigning a most‐likely diagnostic option for anemia, based on evaluating the parameters proposed in this study.
Brianne Morgan, Meghan Langlois, Rachel Schats, Alie E. van der Merwe, Isabelle Ribot, Andrea Waters‐Rist, Megan B. Brickley   +6 more
wiley   +1 more source

Hyperostosis in siblings

South African Medical Journal, 2016
Infantile cortical hyperostosis - Caffey-Silverman disease - is a familial disorder manifesting in the late fetal period or infancy with excessive periosteal bone formation. Signs and symptoms regress spontaneously within months and result in expanded, deformed bones.
Spranger, Jürgen, Lausch, Ekkehart
openaire   +3 more sources

Diffuse idiopathic skeletal hyperostosis in subjects with congestive heart failure undergoing cardiac rehabilitation: A decision tree analysis

Journal of Rehabilitation Medicine
Objective: To assess the prevalence of diffuse idiopathic skeletal hyperostosis and its relationship with vascular risk factors among patients with congestive heart failure. Design: Population-based cross-sectional study.
Pasquale Ambrosino, Domenico Scrutinio, Maurizio De Campi, Enzo Miniero, Roberto Formisano, Giorgio Alfredo Spedicato, Gian Luca Iannuzzi, Nicola Pappone   +7 more
doaj   +1 more source

Melorheostosis of a rib

Radiology Case Reports, 2018
Melorheostos is a rare sclerosing bone dysplasia, characterized by cortical and medullary hyperostosis with typical “dripping candle wax” appearance, usually involving the long bones.
Alexandre Semionov, Rehana Jaffer, John Kosiuk   +2 more
doaj   +1 more source