Results 21 to 30 of about 2,549 (207)

A Rare Case of Oligodontia

Journal of Indian Academy of Oral Medicine and Radiology, 2012
Agenesis of permanent teeth is a congenital abnormality where some of the teeth are missing as the follicles needed for the growth of the teeth are completely absent. Documental evidence of this condition is very limited in literature and the etiology is still obscure.
MLV Prabhuji, Shaeesta Khaleel B Ahmed, K Raghunatha, Vijeev Vasudevan, R Murali, D Devaraju   +5 more
openaire   +3 more sources

Three-dimensional computer-guided implant placement in oligodontia [PDF]

International Journal of Implant Dentistry, 2017
Background The aim of computer-designed surgical templates is to attain higher precision and accuracy of implant placement, particularly for compromised cases.
Marieke A. P. Filius, Joep Kraeima, Arjan Vissink, Krista I. Janssen, Gerry M. Raghoebar, Anita Visser   +5 more
doaj   +2 more sources

Mutations in WNT10B Are Identified in Individuals with Oligodontia [PDF]

The American Journal of Human Genetics, 2016
Supplemental Data Supplemental Data include six figures and three tables and can be found with this article online at http://dx.doi.org/10.1016/j.ajhg.2016.05.012. Supplemental Data Document S1. Figures S1–S6 and Tables S1–S3 Download Document S2.
Yu, Ping, Yang, Wenli, Han, Dong, Wang, Xi, Guo, Sen, Li, Jinchen, Li, Fang, Zhang, Xiaoxia, Wong, Sing-Wai, Bai, Baojing, Liu, Yao, Du, Jie, Sun, Zhong Sheng, Shi, Songtao, Feng, Hailan, Cai, Tao   +15 more
openaire   +4 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

X-Linked Anhidrotic Ectodermal Dysplasia in A 19-Year-Old Male: A Classic Phenotype. [PDF]

Clin Case Rep
ABSTRACT X‐linked anhidrotic/hypohidrotic ectodermal dysplasia (XLHED), also known as Christ‐Siemens‐Touraine syndrome, is a rare genetic disorder characterized by the abnormal development of ectodermal structures, primarily affecting sweat glands, hair, and teeth. It results from mutations in the Ectodysplasin A (EDA) gene.
Chapagain L, Dahal A, Gupta P, Pudasaini P, Paudel U.   +4 more
europepmc   +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

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

Pediatric Dental Management of a Patient With Infantile Osteopetrosis in Remission: A Clinical Case Report. [PDF]

Case Rep Dent
Background Osteopetrosis is a rare genetic disorder characterized by increased bone density due to defective osteoclast function. Its clinical presentation varies according to subtype, and oral manifestations are frequent, potentially serving as early indicators of the disease.
Cruz-Morera MA, Molina-Chaves K, Gomez-Fernandez A.   +2 more
europepmc   +2 more sources

Triad of Micrognathia, Oligodontia, and Ankyloglossia in a Non-Syndromic Individual: A Case Report with Rare Presentation

Journal of Pharmacy and Bioallied Sciences
Deviations from the normal in the intrauterine formative phase have a permanent effect in an individual’s life. They can cause limitations in lifestyle from nil to severe. The sites may differ and hence would the presentations.
Priti Shukla, Varsha Sharma, Shivesh Acharya, Shruti Singh   +3 more
doaj   +2 more sources

Retinal Pigment Epitheliopathy due to Sub-Optimal Recycling of Vitamin A (RESORVA): A Novel RDH11 -Related Phenotype. [PDF]

Clin Genet
RDH11 is a minor isoenzyme that catalyses the oxidation of 11‐cis‐retinol to 11‐cis‐retinal in the retinal pigment epithelium, alongside RDH5 and RDH10. Biallelic null variants in RDH11 lead to upregulation of RDH5 and RDH10 (transcriptional adaptation), maintaining 11‐cis‐retinal bioavailability, but still causing Retinal Pigment Epitheliopathy due to
Stephenson KAJ, Shao Z, Tumber A, Tavares E, Ahmed K, Higginbotham EJ, Marshall CR, Maynes JT, Rajala A, Rajala RVS, Héon E, Vincent A.   +11 more
europepmc   +2 more sources