Results 51 to 60 of about 15,328 (193)

Gingival and Periodontal Diseases and Conditions in Children and Adolescents: Consensus Report

Journal of Clinical Periodontology, Volume 53, Issue 7, Page 1068-1099, July 2026.
ABSTRACT Background The objectives of this Focused Workshop were to update the epidemiology, aetiology, risk factors, diagnosis and management of gingival and periodontal diseases and conditions in children and adolescents, and to explore the applicability of the 2018 Classification in children and adolescents.
Iain Chapple, Sotiria Gizani, Mariano Sanz, Dominique Declerck, Phoebus Madianos, Valerie Clerehugh, Monique Danser, Esti Davidovich, Janet Davies, Nikos Donos, Elisabeth Dursun, Elena Figuero, Filippo Graziani, Mervi Gursoy, Soren Jepsen, Clara Joseph, Moritz Kebschull, Norbert Kraemer, Tina Lambrinaki, Rodrigo López, David J. Manton, Joerg Meyle, Ana Molina, Lior Shapira, Cheryl Somani, Georgios Tsilingaridis, Svante Twetman, Nicola West, Biniyam Wondimu, Ferranti Wong, David Herrera   +30 more
wiley   +1 more source

Accidental Diagnosis of Type VII Osteogenesis Imperfecta in an Infant Presenting With Pneumonia and Rickets‐Like Rib Fractures: A Case Report

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT This case report describes a newborn diagnosed with Type VII Osteogenesis Imperfecta (OI) following an incidental finding of rib fractures during evaluation for pneumonia. The patient presented with multiple fractures, including deformities and callus formations in the ribs and extremities, initially raising concerns for differential diagnoses
Samaneh Parviz, Dariush Hooshyar
wiley   +1 more source

Reduced Dietary Protein Induces Changes in the Dental Proteome

Journal of Experimental Zoology Part B: Molecular and Developmental Evolution, Volume 346, Issue 2, Page 107-127, March 2026.
Low dietary protein (10%) from normal (20%) does change protein expression in tooth proteome and alter developmental pathways. Among the significant protein expressions changes are actin‐based myosins, tooth, and bone development proteins. Perplexingly tooth size is not altered, suggesting more nuanced phenotypic response to low dietary protein in ...
Robert W. Burroughs, Christopher J. Percival, Natasha S. Vitek   +2 more
wiley   +1 more source

Clinical Features of Osteogenesis Imperfecta in Taiwan

Journal of the Formosan Medical Association, 2009
Osteogenesis imperfecta (OI) (MIM 166200, 166210, 259420 and 166220) is a congenital disorder characterized by increased bone fragility and low bone mass. Information regarding the clinical features of this genetic disorder is lacking in Taiwan.
Hsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, Ming-Ren Chen, Chia-Ying Chang, Dau-Ming Niu   +5 more
doaj   +1 more source

Dental Stigmata and Skeletal Lesions of Congenital Treponematosis in Early Agricultural Vietnam (4000–3500 bp)

International Journal of Osteoarchaeology, Volume 36, Issue 2, Page 401-413, March/April 2026.
ABSTRACT Prior research has documented treponematosis at a single site in Mainland Southeast Asia from northern Vietnam dated to the early agricultural transition (~4000–3500 bp). To date, no other cases in Southeast Asia's prehistory have been identified.
Melandri Vlok, Tran Thi Minh, Nicola Czaplinski, Hallie Buckley, Kate Domett, Hiep Hoang Trinh, Nguyen Thi Mai Huong, Nghia Thi Huu, Do Thi Kim Dung, Nguyen Thi Sau, Nguyen Phuong Thao, Do Thi Lan, Phan Thi Kim An, Luong Hong Phuoc, Hirofumi Matsumura, Marc Oxenham   +15 more
wiley   +1 more source

Advances in 3D Printing for Removable Prosthetics—Insights and Perspectives

Journal of Esthetic and Restorative Dentistry, Volume 38, Issue 3, Page 520-529, March 2026.
ABSTRACT Objective This review summarizes recent advances in three‐dimensional (3D) printing for removable prosthodontics, including complete dentures, removable partial dentures, implant‐retained overdentures, and occlusal splints. The aim is to provide clinicians with an overview of current technologies, clinical performance, and future perspectives.
O. Schubert, D. Edelhoff, J. F. Güth, J. Schweiger   +3 more
wiley   +1 more source

Dentinogenesis Imperfecta: Relationship of Genotype with Clinical and Radiographic Features [PDF]

, 2010
Dentinogenesis Imperfecta (DGI) is the most common hereditary anomaly of human dentin. It is typically diagnosed by clinical and radiographic features. It occurs in isolation or in conjunction with the syndrome osteogenesis imperfecta.
Shahangian, Seyed Jossein
core   +1 more source

Dental Hard Tissue Study In A Hereditary Dentinogenesis Imperfecta Family

International Dental Journal
Aim or purpose: Hereditary dentinogenesis imperfecta is a rare autosomal dominant genetic disorder characterized by abnormal dentin structure, leading to impaired dental function and aesthetics.
Zhongren Deng, Yue Ning, Qin Du
doaj   +1 more source

Dentinogenesis Imperfekta : Aspek Genetika Molekular, Klasifikasi dan Upaya Penanggulangannya

Journal of Dentistry Indonesia, 2015
Dentinogenesis Imperfecta (DI) is a hereditary simple autosomal dominant disorder showing abnormalities in the dentin of developing teeth and occuring at a rate of about 1 in 8000 births affecting both primary and secondary dentitions.
Elza Ibrahim Auerkari, A. Surjadi, S. Mangoendjaja   +2 more
doaj   +1 more source

ISOLATED DENTINOGENESIS IMPERFECTA AND IN ASSOCIATION WITH OSTEOGENESIS IMPERFECTA – A LITERATURE REVIEW [PDF]

Romanian Medical Journal, 2018
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic neural crest cells, continuing with their movement towards the first pharyngeal arch and leading to the development of many elements of the ...
Andrei Kozma, Doriana Agop Forna, Viorica Radoi, Ana Maria Alexandra Stanescu, Radu Ursu, Laurentiu Camil Bohaltea   +5 more
doaj   +1 more source