Results 41 to 50 of about 2,035 (211)
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 +17 more
wiley +1 more source
International Journal of Dentistry, Volume 2026, Issue 1, 2026.Objective This study investigated the prevalence of dental anomalies within the athlete population in Qatar using panoramic radiographs. Design This retrospective, cross‐sectional study was conducted at Aspetar Hospital in Qatar. Materials and Methods Digital panoramic radiographs of 5000 records of athletes attending dental department were ...
Atef Hashem +6 more
wiley +1 more source
Dental agenesis in cleft lip and/or palate pf the “Centro Pró-Sorriso” – Universidade José do Rosário Vellano [PDF]
RGO: Revista Gaúcha de Odontologia, 2008 Objective: Analyze periapical and panoramic radiographs in order to define the incidence of dental agenesis in carriers of cleft lip and/or cleft palate among patients of UNIFENAS “Centro Pró-Sorriso” (Pro-Smile Center) in Alfenas – MG.
Orivaldo Tavano +1 more
doaj
Recreating the missing smile: A case report on ectodermal dysplasia
SRM Journal of Research in Dental Sciences, 2012 Ectodermal dysplasia syndrome is a group of hereditary disorders affecting the structures developing from the ectoderm. More than 150 different types have been described with the most common being the hypohidrotic and the hidrotic types.
R Shakila +3 more
doaj +1 more source
Revista da Faculdade de Odontologia de Porto Alegre, 2009 The objective of the present article is to report an uncommon case of a boy with history of 11 natal lost teeth, all belonging to the normal series of primary dentition, associated with absence of up to 21 permanent tooth germs. Such a condition resulted
Patricia Fernanda Dias +3 more
doaj +1 more source
Anhidrotic Ectodermal Dysplasia in a Child Due to a Rare Mutation in the EDA Gene (a Clinical Case)
Журнал медико-биологических исследованийAnhidrotic ectodermal dysplasia is а heterogenous genetic disorder with multiple clinical manifestations. In medical examinations, including dental examinations, the differential aspect of diagnosis is important, since many forms of the disease have ...
Sergey N. Levitskiy +2 more
doaj +1 more source
The Incidence of Tooth Agenesis in Pediatric Patients in the Olomouc Region
Česká Stomatologie a Praktické Zubní Lékařství, 2014 Aim of the study: Many developmental anomalies can occur in craniofacial region. Dental developmental anomalies, namely hypodontia, are the most often of them.
L. Kramerová +3 more
doaj +1 more source
Pigmentary Mosaicism: An Overview
JEADV Clinical Practice, Volume 4, Issue 3, Page 681-689, August 2025.Pigmentary mosaicism is reflected by a patterned hypo‐, hyperpigmentation, or both combined in cutis tricolour. Pigmentary mosaicism can be associated with extracutaneous features (mainly neurological, musculoskeletal or ophthalmological). Three main mechanisms are involved in the development of pigmentary mosaicism: mosaicism for a chromosomal ...
C. Colmant +3 more
wiley +1 more source
Paediatric Hypotrichosis: A Clinical and Algorithmic Approach to Diagnosis
Australasian Journal of Dermatology, Volume 66, Issue 3, Page e109-e119, May 2025.ABSTRACT Paediatric hypotrichosis is the clinical feature of paucity of hair arising congenitally or in early life with the presentation being that of the child whose hair is growing insufficiently. It is a hallmark finding of a diverse group of genodermatoses and sporadic disorders, presenting as either an isolated symptom or in association with ...
Neda So, Leona Yip, David Orchard
wiley +1 more source
Clinical Oral Implants Research, Volume 36, Issue 4, Page 505-517, April 2025.ABSTRACT Objectives WNT10A mutations are associated with tooth agenesis. This study aimed to assess the clinical outcomes of dental implants in patients carrying WNT10A mutations with different molecular statuses and phenotypes over a long‐term follow‐up period. Materials and Methods Patients with tooth agenesis were screened by whole‐exome sequencing (
Jiaqi Dou +6 more
wiley +1 more source