Results 1 to 10 of about 4,161 (209)

Famlial nonsyndromic oligodontia

Contemporary Clinical Dentistry, 2012
Oligodontia is one of the most common developmental abnormalities in humans. The present case report highlights the features of oligodontia in a 12-year-old male patient which was managed successfully with multidisciplinary approach. Familial oligodontia
Punithavathy, John B John, Geetha Priya, Indhumathi Elango, Stalin   +4 more
doaj   +3 more sources

Oligodontia Management in a Resource-Limited Setting: Two Case Reports and Review of Literature [PDF]

Case Reports in Dentistry
Conclusion: Early diagnosis and multidisciplinary management of oligodontia significantly improve functional outcomes and quality of life. Resource limitations necessitated adaptive treatment approaches while maintaining therapeutic efficacy.
A. B. Malami, B. E. Ogbozor, C. C. Okolo, A. O. Aborisade, U. B. Mahmud, A. A. Abulfathi, Y. I. Adeyemo   +6 more
doaj   +2 more sources

Hair Evaluation in Orthodontic Patients with Oligodontia [PDF]

Diagnostics
Oligodontia can be isolated or syndromic, associated with other ectodermal abnormalities. The aim of the study was to perform hair examination in orthodontic patients diagnosed with oligodontia with a low clinical expression of symptoms of ectodermal ...
Małgorzata Zadurska, Adriana Rakowska, Ewa Czochrowska, Małgorzata Laskowska, Konrad Perkowski, Izabela Strużycka, Lidia Rudnicka, Agnieszka Jurek   +7 more
doaj   +2 more sources

Fingerprint Sweat Pore Density in Patients with Oligodontia: A Controlled Clinical Trial [PDF]

Biomedicines
Background/Objectives: There is a lack of evidence for the relationship between sweat pores and tooth agenesis. The aim of this study was to compare sweat pore density on fingertips between a group of patients with oligodontia and a control group without
Jonas Q. Schmid, Jens Reimann, Claudius Middelberg, Ole Oelerich, Thomas Stamm, Ariane Hohoff   +5 more
doaj   +2 more sources

Treatment strategy for patient with non-syndromic tooth agenesis: a case report and literature review [PDF]

BMC Oral Health
Background Non-syndromic tooth agenesis (NSTA) is a type of ectodermal dysplasia (ED) in which patients with non-syndromic oligodontia may only affect teeth. No pathological findings were found in other tissues of the ectodermal. Herein, we report a case
Tianfeng Ouyang, Dong Chen, Zeli Ma, Xin Li, Ge Cao, Lin Lin, Ming Zeng, Ting Chen   +7 more
doaj   +2 more sources

Implant treatment modalities of non-syndromic congenitally missing premolars: a retrospective case series of 74 specialist care patients over an 11-year-cohort [PDF]

Acta Odontologica Scandinavica
Objective: The study aims to evaluate the course of implant treatment for congenitally missing lower ­second premolars in patients referred to publicly funded specialist care over an 11-year period.
Sarwat Jabeen Hassan, Olli-Pekka Lappalainen, Ojala-Alasuutari Marleena, Virpi Harila, Ritva Näpänkangas   +4 more
doaj   +2 more sources

Pre-implant surgery complexity for achieving implant-supported prosthetic rehabilitation in oligodontia patients: a retrospective study [PDF]

BMC Oral Health
Introduction Oligodontia is a rare dental developmental pathology that requires prolonged, complex and multidisciplinary treatment. Although bone augmentation is frequently required during a complete implant treatment of oligodontia.
Ludovic Lauwers, Gwénaël Raoul, Romain Nicot   +2 more
doaj   +2 more sources

A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia. [PDF]

PLoS ONE, 2015
Oligodontia is defined as the congenital absence of six or more permanent teeth, excluding the third molars. Oligodontia may contribute to masticatory dysfunction, speech alteration, aesthetic problems and malocclusion.
Haochen Liu, Tingting Ding, Yuan Zhan, Hailan Feng   +3 more
doaj   +1 more source

Oligodontia and Facial Phenotype Associated with a Rare Syndrome

Case Reports in Dentistry, 2022
Introduction. Oligodontia is a dental abnormality in which the patient is missing teeth. It is a hereditary disorder characterized by agenesis of more than six primary or permanent teeth, excluding the wisdom teeth.
Fatima Ezzahra Zidane, Mustapha El Alloussi   +1 more
doaj   +1 more source

A Nonsyndromic Autosomal Dominant Oligodontia with A Novel Mutation of Pax9-A Clinical and Genetic Report [PDF]

Journal of Clinical and Diagnostic Research, 2015
Oligodontia is congenital absence of one or more teeth which has familial abnormality and attributable to various mutations or polymorphisms of genes often associated with malformative syndromes.
Umapathy Thimmegowda, Praveen Prasanna, Anantharaj Athimuthu, Prasanna Kumar Bhat, Yogish Puttashamachari   +4 more
doaj   +1 more source