Results 51 to 60 of about 301 (154)

Minimally Invasive Cantilever RBFPD Using a 270‐Degree Veneer Abutment in a Young Cleft Patient: A Clinical Adhesive Technique

Clinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Adhesive cantilever resin‐bonded bridges (RBBs) are a minimally invasive option for replacing maxillary lateral incisors in young cleft patients, in whom implant placement is often delayed until completion of craniofacial growth or declined due to surgical burden. Beyond material selection, the outcome depends critically on abutment design and
Aspasia Pachiou, Aikaterini Maria Vraka, Panagiotis Andritsakis, Nikolaos Nikitas Giannakopoulos   +3 more
wiley   +1 more source

Dental agenesis: review of the literature and report of two cases

Revista Facultad de Odontología Universidad de Antioquia, 2006
Tooth agenesis is the most common anomaly of craniofacial development. The purpose of this report is to present a brief review of literature about tooth agenesis, which includes: terminology, etiology, prevalence, associated syndromes and dental ...
Luz Ángela Arboleda-A. , Jacqueline Echeverri-E. , Luz Ángela Restrepo-P. , Martha Lucía Marín-B. , Gonzalo Vásquez-P. , July Catalina Gómez-M., Hugo Alexánder Manco-G. , Clara María Pérez-S. , Elizabeth Taborda-F.   +8 more
doaj  

Anomalias dentárias associadas: o ortodontista decodificando a genética que rege os distúrbios de desenvolvimento dentário Associated dental anomalies: the orthodontist decoding the genetics which regulates the dental development disturbances

Dental Press Journal of Orthodontics, 2010
O presente trabalho versa sobre o diagnóstico e a abordagem ortodôntica das anomalias dentárias, enfatizando os aspectos etiológicos que definem tais irregularidades de desenvolvimento. Parece existir uma inter-relação genética na determinação de algumas
Daniela Gamba Garib, Bárbara Maria Alencar, Flávio Vellini Ferreira, Terumi Okada Ozawa   +3 more
doaj   +1 more source

Carrier screening in the reproductive setting—Are there medical implications for the heterozygote?—A guide for clinicians

Pregnancy, Volume 2, Issue 3, May 2026.
Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld, Nicole Kasatkin, Bi Liu Yu, Milen Velinov, Justin S. Brandt, Elena Ashkinadze   +5 more
wiley   +1 more source

Defeito de desenvolvimento de esmalte em dente permanente resultante de entubação orotraqueal nos primeiros anos de vida [PDF]

RGO: Revista Gaúcha de Odontologia
RESUMO Os defeitos de desenvolvimento de esmalte são alterações resultantes de distúrbios no processo da amelogênese, podendo envolver fatores genéticos, sistêmicos, locais ou ambientais.
Raphaela Magalhães Coimbra, Lucas Porfírio Fernandes Zinis, Ana Emília Farias Pontes, Janaína Cristina Gomes, Rose Mara Ortega   +4 more
doaj   +1 more source

Implant Placement and Immediate Provisionalization After Alveolar Ridge Reconstruction in the Aesthetic Zone Using a Digital Workflow: A 1‐Year Prospective Case Series Study

Clinical Oral Implants Research, Volume 37, Issue 5, Page 543-557, May 2026.
ABSTRACT Introduction In single‐tooth replacement in the aesthetic zone, extensive bone defects require alveolar ridge reconstruction. A digital workflow involving CBCT and intraoral optical scanning enables a three‐dimensional assessment, prosthetically driven implant positioning, computer‐assisted implant surgery, and prefabrication of a temporary ...
Vincent J. J. Donker, Henny J. A. Meijer, Arjan Vissink, Gerry M. Raghoebar   +3 more
wiley   +1 more source

Análisis mutacional del gen MSX1 en pacientes con FLPNS e hipodoncia

Revista Universitas Medica, 2009
Introducción. La etiología de la hendidura labio-palatina es compleja e involucra factores genéticos y ambientales. Además de la hendidura, numerosos estudios han reportado la presencia de anomalías dentales en asociación con varias formas de hendidura ...
SANDRA JANETH GUTIÉRREZ PRIETO, DIANA MARÍA TORRES LÓPEZ, JORGE ARTURO REY CUBILLOS, IGNACIO BRICEÑO BALCÁZAR   +3 more
doaj  

Oral findings in patients with Apert Syndrome Achados bucais em pacientes com Síndrome de Apert

Journal of Applied Oral Science, 2006
INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by mutations in the FGFR2 gene at locus 10q26; patients with this syndrome present severe syndactyly, exophthalmia, ocular hypertelorism and hypoplastic midface ...
Gisele da Silva Dalben, Lucimara Teixeira das Neves, Marcia Ribeiro Gomide   +2 more
doaj   +1 more source

Genotypes and Phenotypes of Patients With TSPEAR‐Related Disorder: Evidence of a Predominant Dental Phenotype

American Journal of Medical Genetics Part A, Volume 200, Issue 4, Page 790-799, April 2026.
ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani, Lucia Tiberi, Annarita Giliberti, Elia Dirupo, Laila Zaroili, Francesco Brancati, Michela Brena, Stefano Caraffi, Chiara De Luca, Livia Garavelli, Anna Virginia Gulino, Milena Mariani, Marzia Pollazzon, Angelo Selicorni, Samuela Landini, Ilaria Sani, Rosangela Artuso, Angela Peron   +17 more
wiley   +1 more source

Early Oral Rehabilitation of a Pediatric Patient With Hypohidrotic Ectodermal Dysplasia: A Case Report from Afghanistan

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Hypohidrotic ectodermal dysplasia (HED) is a rare congenital disorder characterized by abnormal development of ectodermal structures including hair, teeth, nails, and sweat glands. Dental manifestations such as anodontia or hypodontia can significantly impair mastication, speech development, facial esthetics, and psychosocial well‐being ...
Nazera Ahmadzai, Hedayatullah Ehsan, Fatima Sapai, Mohammad Bashir Nejabi, Ahmad Anas Khairzad, Nematullah Sharifi   +5 more
wiley   +1 more source