Results 21 to 30 of about 6,152 (269)

Rehabilitation Considerations for Very Young Children with Severe Oligodontia due to Ectodermal Dysplasia: Report of Three Clinical Cases with a 2-Year Follow-Up

Case Reports in Dentistry, 2022
Introduction. Management of oligodontia can be complicated and requires multidiscipline care, involving a wide spectrum of interventions. The aim of this report is to describe the challenges of oral rehabilitation of three very young children with ...
Kyriaki Seremidi, Antigoni Markouli, Andreas Agouropoulos, Nick Polychronakis, Sotiria Gizani   +4 more
doaj   +2 more sources

AXIN2‐related oligodontia‐colorectal cancer syndrome with cleft palate as a possible new feature

Molecular Genetics & Genomic Medicine, 2023
Background Pathogenic variants in AXIN2 have been associated with tooth agenesis, colon polyps, and colon cancer. Given the rare nature of this phenotype, we set out to collect additional genotypic and phenotypic information.
Laura Roht, Hanne K. Hyldebrandt, Astrid T. Stormorken, Hilde Nordgarden, Rolf H. Sijmons, Dennis K. Bos, Douglas Riegert‐Johnson, Sarah Mantia‐Macklin, Pilvi Ilves, Kai Muru, Monica H. Wojcik, Tiina Kahre, Katrin Õunap   +12 more
doaj   +2 more sources

Familial non-syndromic oligodontia

Journal of Indian Academy of Oral Medicine and Radiology, 2015
Oligodontia, a rare genetic disorder, represents the congenital absence of more than six teeth in primary, permanent, or both dentitions and is usually the feature of a syndrome. Its occurrence as an isolated entity is even rarer.
Seema Basoya, Sridevi Koduri, Ishita Gupta, Vinod Vijay Chandar   +3 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

Oligodontia [PDF]

, 2020
INSERM
openalex   +2 more sources

Genetic Insights into Oligodontia: A Comprehensive Review of Mutations in Key Genes and Their Implications for Tooth Development

International Journal of Current Science Research and Review
Introduction: Tooth agenesis is one of the most frequent congenital abnormalities found in the maxillofacial region. Oligodontia, a severe form of tooth agenesis, occurs as an isolated anomaly or as a syndromic feature.
Pratiwi Soesilowati, Ferhad Ahmad, Fahmi Zakaria Kusnanto   +2 more
semanticscholar   +3 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

Interdisciplinary treatment of ectodermal dysplasia with oligodontia: review and case report

Zdravniški Vestnik, 2013
Background: Ectodermal dysplasia (ED) is a group of hereditary diseases with disorders in the development of two or more ectodermal structures, such as hair, teeth, nails and sweat glands.
Čedomir Oblak, Maja Ovsenik, Nataša Ihan Hren   +2 more
doaj   +1 more source

Non- syndromic oligodontia: A case report

Archives of Dental Research
This case report presents a 14-year-old patient diagnosed with non-syndromic oligodontia, characterized by the absence of multiple permanent teeth. Treatment involved the placement of zirconia crowns in the maxillary arch and a flexi denture in the ...
Roocha Shah, Anup Panda, Mira Virda, Balraj Shukla   +3 more
openalex   +3 more sources

Critical Considerations in Calling Disease-Causing EDAR Mutations in Nonsyndromic Oligodontia. [PDF]

J Clin Med
Background/Objectives: Oligodontia, the absence of six or more teeth excluding third molars, is a rare genetic condition, unlike hypodontia (missing one or more teeth), which is a relatively common human disease. Methods: To identify the genetic etiology
Kim YJ, Gu SY, Chae W, Kim SH, Kim JW.
europepmc   +2 more sources