Results 51 to 60 of about 2,773 (156)

Prosthetic Rehabilitation in Children: An Alternative Clinical Technique

Case Reports in Dentistry, 2013
Complete and partial removable dentures have been used successfully in numerous patients with oligodontia and/or anodontia. However, there is little information in the literature regarding the principles and guidelines to prosthetic rehabilitation for ...
Nádia Carolina Teixeira Marques, Carla Vecchione Gurgel, Ana Paula Fernandes, Marta Cunha Lima, Maria Aparecida Andrade Moreira Machado, Simone Soares, Thais Marchini Oliveira   +6 more
doaj   +1 more source

Familial Adenomatous Polyposis—Risk of Cancer, Cancer Prevention, and Long‐Term Consequences: Learnings from Five Decades with the Danish Polyposis Register

APMIS, Volume 134, Issue 5, May 2026.
ABSTRACT Familial adenomatous polyposis (FAP) is a hereditary condition marked by the growth of hundreds to thousands of adenomatous polyps in the colon and rectum, significantly elevating the risk of colorectal cancer (CRC) if left untreated. Caused by pathogenic variants in the APC gene, FAP is typically identified in adolescence, often leading to ...
John Gásdal Karstensen
wiley   +1 more source

Interim three-dimensional printed overlay prosthesis for an adolescent patient with oligodontia

The Journal of Indian Prosthodontic Society, 2021
Oligodontia is a developmental anomaly which represents the congenital absence of more than six teeth in primary, permanent, or both dentitions and may or may not be associated with a syndrome.
Deepa Mukkai Krishnamurthy, Rajeev Singh, Gaurang Mistry   +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

Early treatment of nonsyndromic oligodontia: a clinical case report

Bioscience Journal, 2017
This report aims to describe the clinical case of a 10-year-old male patient (R.C.B.C.), presenting nonsyndromic oligodontia with maternal family trait and absence of 22 permanent teeth.
Carolina Ribeiro Starling, Caroline Mathias Carvalho de Souza, Rogério Frederico Alves Ferreira, Marcos Alan Vieira Bittencourt   +3 more
doaj   +3 more sources

Tooth agenesis review

Česká Stomatologie a Praktické Zubní Lékařství, 2012
Background: Tooth agenesis means absence or incomplete development of tooth. It is a common human anomaly, which according to Online Mendelian Inheritance in Man database affects approximately 20% of the population.
L. Gábrlíková
doaj   +1 more source

Early prosthetic rehabilitation of severe oligodontia with implant–retained overdenture: A case report

Zdravniški Vestnik, 2020
Background: Ectodermal dysplasia is a rare hereditary disease, characterized by defects in the development of two to five tissues derived from the embryonic ectoderm. As a part of the manifestation, oligodontia can occur.
Sonja Zarkovic Gjurin, Nataša Ihan Hren, Tanja Tomaževič, Čedomir Oblak   +3 more
doaj   +1 more source

Oligodontia severa em paciente não sindrômico : relato de caso clínico [PDF]

, 2015
Introdução: Chama-se Oligodontia a agenesia congênita de seis ou mais dentes, excluindo os terceiros molares. Geralmente apresenta-se em pacientes com envolvimento sindrômico, mas também pode ser encontrada de forma isolada Objetivo: O presente trabalho ...
Noal, Fernanda Coradini
core   +1 more source

Prevalence and Patterns of Permanent Tooth Agenesis in Patients With Crouzon or Apert Syndrome: A Systematic Review and Meta‐Analysis

Orthodontics &Craniofacial Research, Volume 29, Issue 1, Page 1-11, February 2026.
ABSTRACT Crouzon and Apert syndromes are rare syndromic craniosynostoses frequently associated with craniofacial and dental anomalies, including tooth agenesis. Although individual studies have reported tooth agenesis prevalence data in specific populations, no attempts have been made to systematically synthesise these data.
M. Cecilia Becerril Santos, Edwin M. Ongkosuwito, Alexandra K. Papadopoulou, Gregory S. Antonarakis   +3 more
wiley   +1 more source