Results 81 to 90 of about 596,467 (176)

Associated dental anomalies: the orthodontist decoding the genetics which regulates the dental development disturbances [PDF]

, 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
ALENCAR, Bárbara Maria, Terumi Okada Ozawa, FERREIRA, Flávio Vellini, GARIB, Daniela Gamba, Flávio Vellini Ferreira, OZAWA, Terumi Okada, Daniela Gamba Garib, Bárbara Maria Alencar, Ozawa,Terumi Okada, Garib,Daniela Gamba, Alencar,Bárbara Maria, Ferreira,Flávio Vellini   +11 more
core   +1 more source

Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria

American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2181-2198, October 2026.
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy, Jesse Richards, Brooke R. Sweeney, Seema Kumar, Katie E. Queen, Joshua Zaritsky, Carl H. Cramer, Elias I. Traboulsi, Brittni A. Scruggs, Erica E. Davis, Ekaterina Keifer, Emma McGibbon, Timothy Ogden, Bendert De Graaf, Tonia Hymers, Elizabeth Forsythe, Philip Beales   +16 more
wiley   +1 more source

Bases moleculares de la agenesia dental no sindrómica: revisión de la información bibliográfica Molecular bases of non syndromic dental agenesis: review of the literature

Revista de la Asociación Odontológica Argentina, 2013
Resumen Este trabajo pretende actualizar los conocimientos acerca de las bases moleculares de la agenesia dental no sindrómica. Más de doscientos genes codifican múltiples proteínas con funciones necesarias para el desarrollo dental.
Clara Teicher, Alejandrina Valvo, Alicia Nannini   +2 more
doaj  

De Novo 2.2 Mb 19q13.42–q13.43 Microdeletion Encompassing U2AF2: Support for a Haploinsufficiency Model

American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2350-2356, October 2026.
ABSTRACT U2 small nuclear RNA auxiliary factor 2 (U2AF2) is an essential pre‐mRNA splicing factor involved in the early stages of pre‐mRNA splicing. To date, multiple individuals have been reported with predominantly heterozygous missense variants presenting intellectual disability, speech and motor delays, seizures, hypotonia, and thin or hypoplastic ...
Amanda Toledo, Sarah Araji, Weimin Bi, Seema R. Lalani   +3 more
wiley   +1 more source

Craniofacial Morphology and Dental Age Assessment in Pediatric Craniosynostosis: A Comparative Cross‐Sectional Study

Clinical and Experimental Dental Research, Volume 12, Issue 5, October 2026.
ABSTRACT Objectives To delineate the craniofacial morphometric characteristics of Thai children with syndromic (SC) and non‐syndromic craniosynostosis (NSC) and to assess dental maturation relative to Chronological Age (CA). Methods This comparative cross‐sectional study evaluated 19 patients (SC: n = 13; NSC: n = 6; mean age 9.32 ± 2.67 years ...
Nutthakarn Ratanasereeprasert, Yanisa Wongbanthit, Narin Intarak, Preeya Suwanwitid, Chutimont Teekavanich, Anand Marya, Guang Hong, Thantrira Porntaveetus   +7 more
wiley   +1 more source

Tooth agenesis: part 1. Incidence and diagnosis in orthodontics.

, 2019
Dental agenesis has a great clinical significance due to its frequency during daily practice and the therapeutic problems that can arise from it. This paper will explore the incidence of dental agenesis, its diagnosis and how this anomaly affects the ...
Nocini, P F., De Santis, D, Matarese, M, Ricciardi, G, Nocini, R, Sinigaglia, S, Luciano, U, Lucchese, A, Donadello, D, Pancera, P, Bertossi, D, Kumar, N, Zotti, F, Albanese, M, Croce, S, Faccioni, P   +15 more
core  

Coexistence of tooth agenesis and ovarian cancer — a systematic literature review [PDF]

, 2019
Objectives: Dental agenesis — a congenital lack of teeth — is one of the most frequently diagnosed developmentaldefects of dentition. Genetics is a crucial factor in the etiology of this disorder. Missing teeth can be caused by mutationin genes including
Pitynski, Kazimierz; Department of Gynecology and Obstetrics, Faculty of Medicine, Jagiellonian University Medical College, Cracow, Poland, Spaczynska, Joanna; Department of Gynecology and Obstetrics, Faculty of Medicine, Jagiellonian University Medical College, Cracow, Poland, Gawron-Jakubek, Weronika; Department of Orthodontics, Dental Institute, Faculty of Medicine, Jagiellonian University Medical College, Montelupich St. 4, 31-155 Kraków, Poland, Loster, Bartlomiej W.; Department of Orthodontics, Dental Institute, Faculty of Medicine, Jagiellonian University Medical College, Montelupich St. 4, 31-155 Kraków, Poland, Gawron-Jakubek, Weronika, Spaczyńska, Joanna, Pityński, Kazimierz, Loster, Bartłomiej   +7 more
core   +2 more sources

Association between tooth agenesis and developmental dental anomalies: an observational study with machine learning analysis [PDF]

Dental Press Journal of Orthodontics
Objective: To investigate the prevalence of tooth agenesis and its association with other developmental dental anomalies in non-syndromic patients.
Guilherme Henrique BORGES, Walbert A. VIEIRA, Isabela Vinhal HENRIQUES, Lígia Machado SILVA, Rubens SPIN-NETO, Marcos Alan Vieira BITTENCOURT, Luiz Renato PARANHOS   +6 more
doaj   +2 more sources

Dentofacial Characteristics in Patients With Epidermolysis Bullosa—A Cross‐Sectional Study

Clinical and Experimental Dental Research, Volume 12, Issue 5, October 2026.
ABSTRACT Objectives Epidermolysis bullosa (EB) is a rare genetic disease characterized by skin and mucosal fragility caused by pathogenic variants in structural protein genes. Malocclusions have been previously described in patients with EB, mainly in case reports, with no cohort studies characterizing dentofacial characteristics across all EB types ...
Sebastián Véliz, Susanne Krämer, Colomba Besa‐Witto, Pedro Diz‐Dios   +3 more
wiley   +1 more source

Grem2 Deficiency Disrupts Msc Homeostasis Leading To Tooth Agenesis

International Dental Journal
Aim or purpose: Nonsyndromic tooth agenesis/hypodontia represents the most prevalent human dental developmental disorder. While GREMLIN 2 (GREM2) mutations are clinically linked to isolated tooth agenesis, microdontia, and taurodontism, their pathogenic ...
Qiongyu Zhang, Changchun Dong
doaj   +1 more source