Results 51 to 60 of about 2,550 (192)

Prevalence, Characteristics, and Predictive Factors of Dentoalveolar and Spreading Odontogenic Infections in Children Treated Under General Anaesthesia

International Journal of Paediatric Dentistry, Volume 36, Issue 1, Page 13-18, January 2026.
ABSTRACT Background Children receiving dental treatment under general anesthesia (GA) often have odontogenic infections (OIs). Early detection and treatment of patients at risk of OIs can improve oral health and prevent early tooth extractions. Aim To investigate the prevalence, characteristics, and predictive factors of OIs in children receiving ...
Annmari Hyppänen, Fanny Mussalo, Johanna Snäll, Heikki Alapulli, Eija Salmela   +4 more
wiley   +1 more source

Epidemiological and Clinical Features of Regional Odontodysplasia in South Korean Pediatric Patients: A Multicenter Case Series Study

International Journal of Paediatric Dentistry, Volume 36, Issue 1, Page 140-152, January 2026.
ABSTRACT Background Regional odontodysplasia (RO) is a rare developmental dental anomaly with unknown prevalence. Current knowledge is largely limited to individual case reports. Aim This study aims to present epidemiological data, clinical features, and radiographic characteristics of pediatric and adolescent patients with RO in South Korea. Design In
So Dam Lee, Je Seon Song, Hyo Seoul Lee, Hyuntae Kim, Yeonmi Yang, Ko Eun Lee   +5 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 [PDF]

Clin Case Rep
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
Parviz S, Hooshyar D.
europepmc   +2 more sources

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

Expanding the Clinical Spectrum of Bruck Syndrome: A Case Report and Literature Review

Case Reports in Pediatrics, Volume 2026, Issue 1, 2026.
Background Bruck syndrome is a rare autosomal recessive disorder characterized by osteogenesis imperfecta–like bone fragility and congenital joint contractures. Clinical overlap with other connective tissue disorders makes early diagnosis challenging, and genetic testing remains essential.
Ansam Nafah, May Shihab, Reem Shihab, Lana M. Dweekat, Hala O. Abdallah, Andrea Scaramuzza   +5 more
wiley   +1 more source

Three Decades of Enamel Matrix Derivative: From Dental Innovation to Extra‐Oral Applications

International Journal of Dentistry, Volume 2026, Issue 1, 2026.
Introduction Enamel matrix derivative (EMD; Emdogain) has been deployed for three decades as a biologically active material in periodontal regeneration. Widely adopted in periodontology, its indications are expanding into endodontics, ridge preservation, implantology, dermatology and oncology‐related indication.
Faustino Mercado, Carolina Loch, Ahmad Mustafa, Euna Lee, Michelle Hecker, Hannah Wesley   +5 more
wiley   +1 more source

DS_10.1177_0022034519854029 – Supplemental material for Mutant Dentin Sialophosphoprotein Causes Dentinogenesis Imperfecta

, 2019
Supplemental material, DS_10.1177_0022034519854029 for Mutant Dentin Sialophosphoprotein Causes Dentinogenesis Imperfecta by T. Liang, H. Zhang, Q. Xu, S. Wang, C. Qin and Y.
T. Liang (6814781), Q. Xu (696095), Y. Lu (1469287), H. Zhang (537656), C. Qin (6814784), S. Wang (673797)   +5 more
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

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

Clinical and Molecular Heterogeneity Underlying Monogenic Causes of Pediatric Diabetes Associated to Brain Developmental Disorders

Clinical Genetics, Volume 108, Issue 5, Page 495-510, November 2025.
A growing number of genetic variants linking non‐autoimmune diabetes to NDDs across different ages offer key insights about a common background of these phenotypes. These findings call for multidisciplinary approaches to care that integrate metabolic and neurological management in affected children.
Gabriele Di Pasquale, Camilla Valsecchi, Giulia Marie Smylie, Vincenzo Salpietro, Gian Vincenzo Zuccotti, Maurizio Delvecchio, Chiara Mameli   +6 more
wiley   +1 more source