Results 61 to 70 of about 2,035 (211)

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

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

Frequency, prevalence and treatment methods of anodontia and supernumbered teeth [PDF]

, 2023
Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”, Chişinău, Republica MoldovaIntroducere. Anodonțiile și dinții supranumerari sunt anomalii dentare de număr, care se întâlnesc cu o frecvență de la 0,5% până la 12,5%.
Stepco, Elena, Globa, Mihai
core  

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  

Congenital hypotrichosis and partial anodontia in a crossbred beef calf

, 2007
Clinical examination, skin biopsies, skull radiographs, and DNA analysis of a 2-day-old Red Angus-Charolais-Simmental cross bull calf confirmed the diagnosis of congenital hypotrichosis and anodontia defect (HAD), also called anhidrotic ectodermal ...
Palmer, Colin W, Barlund, Christy S, Clark, Edward G, Leeb, Tosso, Drögemüller, Cord   +4 more
core  

Prevalence of anodontia in 2nd level students in Sao Jose dos Campos-correlation between third molar anomalies and other teeth [PDF]

, 1990
The authors studied 201 school children form both sexes, aging 12 to 14 years, in order to identify anodontia, including in third molars. The results indicated a congenital absence of teeth in 24.37% of the examined children, distributed into 10.44% of ...
de Melo Castilho, J. C., Nicodemo, R. A., Bazzarella, C. B., de Moraes, L. C.   +3 more
core  

Conservative interdisciplinary management for a congenitally missing maxillary lateral incisor in an adolescent patient

Australian Dental Journal, Volume 69, Issue 4, Page 267-277, December 2024.
Abstract A congenitally missing lateral incisor tooth is commonly associated with both short and long‐term clinical dilemmas, particularly for a growing patient. A unilaterally missing maxillary lateral incisor tooth creates a significant dental asymmetry in the critical aesthetic zone of the smile and potentially increases the difficulty of any ...
R Hmud, DC‐V Ong
wiley   +1 more source

Prosthetic management of an 11-year-old patient with hereditary ectodermal dysplasia and partial anodontia – a case report.

, 2010
Objective: To illustrate the problems of partial anodontia and replacement of missing teeth and bone in patients with ectodermal dysplasia.Method: The illustrative case is an 11year old boy with tuberculoid shaped 11, 21 and 16 as the teeth present in ...
Akeredolu, P.A, P.A Akeredolu, A.C.O Olojede, Olojede, A.C.O   +3 more
core   +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

Whole genome sequencing in families with oligodontia

Oral Diseases, Volume 30, Issue 6, Page 3935-3950, September 2024.
Abstract Background/Objectives Tooth agenesis (TA) is among the most common malformations in humans. Although several causative mutations have been described, the genetic cause often remains elusive. Here, we test whether whole genome sequencing (WGS) could bridge this diagnostic gap.
Janna Mitscherling, Henrike L. Sczakiel, Olga Kiskemper‐Nestorjuk, Sibylle Winterhalter, Stefan Mundlos, Theodosia Bartzela, Martin A. Mensah   +6 more
wiley   +1 more source