Results 51 to 60 of about 1,605 (178)

The Incidence of the Tooth Agenesis in Students of Dentistry at Palacký University in Olomouc

Česká Stomatologie a Praktické Zubní Lékařství, 2015
Aim of the study: Tooth agenesis is very often developmental anomaly. The prevalence of this disorder differs depending on several factors. Different results can be observed in populations on different continents, in different races and genders, and in ...
L. Kramerová, P. Krejčí, K. Langová, A. Ševecová   +3 more
doaj   +1 more source

Ectodermal dysplasia with true anodontia

Journal of Oral and Maxillofacial Pathology, 2011
The hereditary condition known as ectodermal dysplasia is characterized by the absence or defect of two or more ectodermally derived structures. The most commonly observed forms of ectodermal dysplasia are the hidrotic and hypohidrotic types; discrimination is based on the absence or presence of sweat glands.
Bala, Madhu, Pathak, Anuradha
openaire   +3 more sources

A Rare Case Report of a Large Dentigerous Cyst in the Maxillary Sinus Associated With an Ectopic Maxillary Third Molar

Case Reports in Dentistry, Volume 2025, Issue 1, 2025.
Ectopic eruption of permanent molars is an uncommon developmental anomaly characterized by abnormal tooth positioning, which can lead to significant complications. In rare instances, ectopic molars may be associated with dentigerous cysts, particularly within the maxillary sinus, posing challenges for diagnosis and management.
Marika Ramishvili, Leila Atskvereli, Giorgi Menabde, Marika Zurmukhtashvili, Sopio Samkharadze, Giorgi Dugashvili, Luc Marks, Paulo J. Palma   +7 more
wiley   +1 more source

Hypodontia in the permanent dentition: a study of its prevalence in Malaysian children

Australasian Orthodontic Journal, 1989
An investigation of the prevalence and distribution of hypodontia was carried out in Malaysian children between the ages of five to fifteen years. Hypodontia occurred in 2.8 per cent of these children.
Nik-Hussein Nik Moriah
doaj   +1 more source

Displasia Ektodermal Hipohidrotik

Sari Pediatri, 2016
Seorang bayi laki-laki berusia 4 bulan menderita displasia ektodermal hipohidrotik (DEH), merupakan kelainan genetik yang sebagian besar diturunkan secara x-linked recessive.
Eveline PN, Sri Rezeki Hadinegoro, Siti Aisah Boediardja   +2 more
doaj   +1 more source

Oligodontia Management in a Resource‐Limited Setting: Two Case Reports and Review of Literature

Case Reports in Dentistry, Volume 2025, Issue 1, 2025.
Introduction: Oligodontia represents the developmental absence of six or more teeth, posing significant challenges for masticatory function, speech, and psychosocial well‐being. While extensively documented in developed countries, limited reports exist from resource‐constrained settings in Africa.
A. B. Malami, B. E. Ogbozor, C. C. Okolo, A. O. Aborisade, U. B. Mahmud, A. A. Abulfathi, Y. I. Adeyemo, Hannah Wesley   +7 more
wiley   +1 more source

Ectodermal Dysplasia - Connections and Implantation

Česká Stomatologie a Praktické Zubní Lékařství, 2009
Ectodermal dysplasia is a disease of strong familial disposition. There is a broad scale of subtypes with more or less expressed signs. The diagnostics is of high significance as well as the associated missing teeth.
P. Prachár, S. Bartáková, P. Černochová, J. Kuklová, J. Vaněk   +4 more
doaj  

Case Report of a Novel EVC Gene Mutation in Ellis–van Creveld Syndrome: Implications for Pediatric Dental Management

Case Reports in Dentistry, Volume 2025, Issue 1, 2025.
Introduction Ellis–van Creveld (EVC) syndrome, also known as chondroectodermal dysplasia, is a rare autosomal recessive disorder that affects multiple embryonic tissues. It is primarily caused by mutations in the EVC gene. Patient Information We report an 11‐year‐old male diagnosed with EVC syndrome, who carries a novel homozygous pathogenic mutation ...
Mahnegar Shariati, Sara Tavassoli-Hojjati, Amirahmad Pahlavan Hoseini, Hanieh Jadidi, Hannah Wesley   +4 more
wiley   +1 more source

DCAF17 Mutation in Woodhouse–Sakati Syndrome: A Case Report on a Novel Homozygous Variant

Case Reports in Pediatrics, Volume 2025, Issue 1, 2025.
Background: Woodhouse–Sakati syndrome (WSS) is a rare autosomal recessive disorder characterized by a constellation of symptoms, including alopecia, hypogonadism, diabetes, mental retardation, and extrapyramidal syndrome. Here, we present a case study of a girl with WSS, focusing on clinical features, genetic analysis, and treatment.
Asal Khalili Dehkordi, Rahim Vakili, Juan Manuel Mejía-Aranguré   +2 more
wiley   +1 more source

Customized Prosthetic Oral Rehabilitation of a Child with Hypohidrotic Ectodermal Dysplasia: A Case Report [PDF]

Journal of South Asian Association of Pediatric Dentistry
The present case report describes interdisciplinary prosthetic oral rehabilitation of a 7-year-old male child presenting classical features of hypohidrotic ectodermal dysplasia (HED) and subtotal anodontia. The treatment, in this case, was simplified and
Hitesh Chander Mittal, Sudhir Bhandari, Ashima Goyal, Aditi Kapur, Krishan Gauba   +4 more
doaj   +1 more source