Results 51 to 60 of about 2,549 (207)

Full Mouth Rehabilitation of an Adolescent Patient with Ectodermal Dysplasia: A Case Report [PDF]

Journal of South Asian Association of Pediatric Dentistry, 2022
Ectodermal dysplasia comprises genetic disorders of divergent groups that include dystrophies of ectodermally derived structures and their accessory structures, including hair, glands, teeth, skin, and nails.
Amith Adyanthaya, Aparna Sivaraman, CR Sangeetha, Reshma Aloysius, K Risana, Swetha S Nair   +5 more
doaj   +1 more source

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   +1 more source

Concurrent manifestation of oligodontia and thrombocytopenia caused by a contiguous gene deletion in 12p13.2: A three‐generation clinical report

Molecular Genetics & Genomic Medicine, 2019
Background Wnt and Wnt‐associated pathways play an important role in the genetic etiology of oligodontia, a severe form of tooth agenesis. Loss‐of‐function mutations in LRP6 , encoding a transmembrane cell‐surface protein that functions as a coreceptor ...
Jamila Ross, Willem Fennis, Nicole deLeeuw, Marco Cune, Annemieke Willemze, Antoine Rosenberg, Hans‐Kristian Ploos van Amstel, Marijn Créton, Marie‐José van denBoogaard   +8 more
doaj   +1 more source

Prosthetic rehabilitation of oligodontia in a child: a case report

Update Dental College Journal, 2014
Oligodontia is a developmental dental anomaly. It is either an isolated trait or part of a syndrome. Oligodontia is characterized by the congenital absence of more than six permanent teeth except the third molars.
Rubaba Ahmed, Md Ashik Rayhanb, Atiquzzaman Khan, Md Masudur Rahman   +3 more
doaj   +1 more source

Oligodontia with taurodontism in monozygous twins

North American Journal of Medical Sciences, 2012
Dear Editor, A wide spectrum of developmental pathologies affects the teeth, which includes variation in shape, size, eruption pattern, and number. Tooth agenesis is one such condition that leads to hypodontia and oligodontia. Prevalence of hypodontia was found to be 1.6% to 9.6% in the permanent dentition.
Kandagal, V Suresh, Bilahari, N, Shenai, Prashanth, Chatra, Laxmikanth, Pramod, R C, Ashir, K R   +5 more
openaire   +3 more sources

The oligodontia phenotype in a X-linked hypohidrotic ectodermal dysplasia patient with a novel EVC2 variant

Heliyon
Objectives: To analyse the pathogenic genes in a patient with hypohidrotic ectodermal dysplasia (HED) and explore the relationship between pathogenic genes and the oligodontia phenotype.
Yi Wu, Jing Sun, Caiqi Zhang, Siyuan Ma, Yiting Liu, Xiaoshan Wu, Qingping Gao   +6 more
doaj   +1 more source

Periodontal Architecture in Ectodermal Dysplasia: An Observational Clinical and Histological Study

Oral Diseases, EarlyView.
ABSTRACT Objective To investigate gingival and periodontal characteristics in Ectodermal dysplasia (ED), focusing on soft‐tissue phenotype, anatomical variations, and periodontal architecture. Materials and Methods Observational clinical study of 11 individuals (16–30 years) with confirmed clinical or genetic ED diagnosis.
Marco Montevecchi, Margherita Giorgia Liguori, Ilaria Santini, Nicola Marco Sforza, Giulia Querzoli, Leoluca Valeriani   +5 more
wiley   +1 more source

Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population. [PDF]

PLoS ONE, 2013
BACKGROUND: Dental agenesis is the most common, often heritable, developmental anomaly in humans. Although WNT10A gene mutations are known to cause rare syndromes associated with tooth agenesis, including onycho-odontodermal dysplasia (OODD), Schöpf ...
Huiying He, Dong Han, Hailan Feng, Hong Qu, Shujuan Song, Baojing Bai, Zhenting Zhang   +6 more
doaj   +1 more source

Molecular Basis and Clinical Spectrum of WNT10A‐Related Oligodontia

Clinical Genetics, Volume 110, Issue 1, Page 3-14, July 2026.
Cellular Mechanism behind WNT10A phenotypes. ABSTRACT WNT10A mutations, a major genetic determinant of dental agenesis and ectodermal dysplasia, exert profound effects on craniofacial development. Although classified as rare disorders, these mutations account for more than half of oligodontia cases, reflecting their critical role.
Perennes Elise, Benkirane‐Jessel Nadia, Anton Nicolas, Vandamme Thierry, Clauss François, Conzatti Guillaume   +5 more
wiley   +1 more source

Dental management of a pediatric patient with progressive familial intrahepatic cholestasis having dental anomalies: a case report and brief review of the literature

BMC Oral Health, 2023
Background Progressive familial intrahepatic cholestasis is a heterogeneous group of disorders, leading to intrahepatic cholestasis, with the possibility of chronic liver failure and biliary cirrhosis.
Mina Yazdizadeh, Maryam Sharifi, Arefeh Torabi Parizi, Firoozeh Alipour, Maryam Ghasempuor, Elham Zanguei, Maryam Yazdizadeh   +6 more
doaj   +1 more source