Results 91 to 100 of about 127,214 (299)

The Twin‐Rooted Anomaly: Endodontic Management of a Rare Case of a Maxillary Central Incisor With Two Roots

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT This case report describes the endodontic management of a maxillary central incisor with two roots, representing a rare anatomical variation. A 73‐year‐old female patient presented with a fractured tooth #21 with a carious crown. Pulp sensibility testing using cold spray elicited a sharp and prolonged painful response, consistent with a ...
Mohsen Aminsobhani, Maryam Babaahmadi
wiley   +1 more source

Malnutrition, enamel defects, and early childhood caries in preschool children in a sub-urban Nigeria population.

PLoS ONE, 2020
OBJECTIVES:The study tried to determine if malnutrition (underweight, stunting, wasting, overweight) and enamel defects (enamel hypoplasia, hypomineralized second molar, amelogenesis imperfecta, fluorosis) were associated with early childhood caries (ECC)
Morenike Oluwatoyin Folayan, Maha El Tantawi, Ayodeji Babatunde Oginni, Michael Alade, Abiola Adeniyi, Tracy L Finlayson   +5 more
doaj   +1 more source

Factors influencing oral colonization of mutans streptococci in young children [PDF]

, 2007
The document attached has been archived with permission from the Australian Dental Association. An external link to the publisher’s copy is included.This paper aims to critically review current knowledge about the key factors involved in oral ...
Law, V., Seow, W., Townsend, G.
core   +1 more source

Bilateral Symmetrical Fusion of Permanent Mandibular Lateral Incisors and Canines: A Rare Clinical Case

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Fusion is a rare developmental anomaly characterized by the union of two adjacent tooth germs during the morphodifferentiation stage of tooth formation, resulting in a single enlarged tooth. Its prevalence ranges from 0.4% to 0.9% in the primary dentition and approximately 0.2% in the permanent dentition.
Suresh Kandagal Veerabhadrappa, Jayanth Kumar Vadivel, Mohamed Zahoor Ul Huqh, Siddharthan Selvaraj, Anand Marya, Seema Yadav   +5 more
wiley   +1 more source

Prevalence and clinical characteristics of molar incisor hypomineralization in Erbil City, Iraq

Journal of Indian Society of Pedodontics and Preventive Dentistry
Objective: To determine the prevalence, severity, and clinical characteristics of molar incisor hypomineralization (MIH) among children in Erbil City, Iraq, and its relation to enamel hypoplasia in the primary teeth.
Bushra Rashid Noaman, Layla Mohammed Fattah, Zaineb Yalman Othman, Sara Sherzad Rasool   +3 more
doaj   +1 more source

Enamel hypoplasia or amelogenesis imperfecta - a restorative approach

Brazilian Journal of Oral Sciences, 2015
Genetic or acquired disturbances may lead to the development of alterations on enamel structure, compromising tooth esthetics and function. This short communication aims to briefly discuss the possibility of employment of several treatment options either
Rodrigo Borges Fonseca, Lourenço Correr Sobrinho, Alfredo Júlio Fernandes Neto, Adérito Soares Mota, Carlos José Soares   +4 more
doaj   +1 more source

Type 1 Diabetes and Other Autoimmune Diseases—Epidemiology, Pathophysiology and Screening

Endocrinology, Diabetes &Metabolism, Volume 9, Issue 1, January 2026.
Individuals with type 1 diabetes exhibit significantly increased prevalence of additional autoimmune diseases. Epidemiological, familial and mechanistic evidence indicates frequent polyautoimmunity and shared genetic and environmental drivers. Coexistence complicates clinical management, and autoantibody‐based detection often identifies preclinical ...
George J. Kahaly, Thomas Forst, Monika Kellerer, Stefanie Lanzinger, René D. Rötzer, Matthias Schott, Petra‐Maria Schumm‐Draeger   +6 more
wiley   +1 more source

CDG due to Defective Membrane Transporters: Update

Journal of Inherited Metabolic Disease, Volume 49, Issue 1, January 2026.
ABSTRACT Congenital disorders of glycosylation are genetic defects in the glycoprotein and glycolipid glycan assembly and attachment. Some 200 CDG have been reported since the first clinical description in 1980. Most CDG are enzymatic deficiencies, but 13 (6.5%) are defects in the ER, Golgi apparatus (GA), and plasma membrane transporters.
D. Quelhas, C. R. Ferreira, J. Jaeken
wiley   +1 more source

A novel MBTPS2 missense variant identifying keratosis follicularis spinulosa decalvans in a case of neonatal erythroderma

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Edwin Cuperus, Michel van Geel, Virginie JM Verhoeven, Suzanne M Koudijs, Gerharda H Boerman, Angela M Tjiam, N Margreth van der Lugt, Suzanne GMA Pasmans   +7 more
wiley   +1 more source

Assessment of Alterations in Permanent Premolars After Endodontic Treatment of Predecessor Primary Molars: A Prospective Study

International Journal of Paediatric Dentistry, Volume 36, Issue 1, Page 33-39, January 2026.
ABSTRACT Background The relationship between primary teeth and their successors involves complex interactions that may influence the development of permanent teeth. Aim To evaluate alterations in permanent premolars after endodontic treatment of their primary molar predecessors. Design A prospective study was conducted with children initially aged 5 to
Rafaela Lourdes de Sousa, Elisa Varela de Oliveira, Josiane Pezzini Soares, Nashalie Alencar, Jéssica Barasuol, Pablo Silveira Santos, Mariane Cardoso, Michele Bolan   +7 more
wiley   +1 more source