Results 41 to 50 of about 2,260 (205)

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

, 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

Prosthodontic management of anhidrotic ectodermal dysplasia

Indian Journal of Dental Research, 2011
Ectodermal dysplasia is characterized by the absence or defects of two or more ectodermally derived structures. Anodontia or hypodontia is the most striking dental manifestation. In severe hypodontia, there is lack of alveolar development with consequent
Shilpy Gupta, Parimala Tyagi
doaj   +1 more source

AGE PECULIARITIES OF PROOXIDANT-ANTIOXIDANT BALANCE OF THE ORAL FLUID IN PATIENTS AGAINST THE BACKGROUND OF INTAKT DENTITIONS, PARTIAL AND COMPLETE ANODONTIA [PDF]

, 2022
Relevance. The study is conditioned by a steady tendency of demographic aging of the population. On the part of the dental system, one of the most common age-related disorders is the tooth loss and the necessity to replace dentition defects.
O.Ya. Barabash
core   +1 more source

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   +1 more source

Early prosthodontic intervention in a child patient of hypohidrotic ectodermal dysplasia

SRM Journal of Research in Dental Sciences, 2013
The ectodermal dysplasias (EDs) comprise a large, heterogeneous group of inherited disorders that are defined by primary defects in the development of two or more tissues derived from embryonic ectoderm.
Culatur Thulasingam, Meenakshi Akshayalingam, Pallavi Vashisht   +2 more
doaj   +1 more source

Intrafamilial Phenotypic Variability and Dental Management of Ectodermal Dysplasia in Three Siblings: A Case Report

Case Reports in Dentistry, Volume 2026, Issue 1, 2026.
Ectodermal dysplasia (ED) is a heterogeneous group of inherited disorders affecting ectoderm‐derived structures, with dental anomalies representing a major clinical concern. This case report describes three siblings from a Tunisian family presenting marked intrafamilial phenotypic variability of ED.
Farah Chouchene, Fatma Masmoudi, Ahlem Baaziz, Andrea Scribante   +3 more
wiley   +1 more source

Implants in adolescents

Journal of Indian Society of Periodontology, 2013
Implants have gained tremendous popularity as a treatment modality for replacement of missing teeth in adults. There is extensive research present on the use of implants in adults, but there is a dearth of data available on the same in adolescents.
Rohit A Shah, Dipika K Mitra, Silvia V Rodrigues, Pragalbha N Pathare, Rajesh S Podar, Harshad N Vijayakar   +5 more
doaj   +1 more source

Prevalence and Patterns of Five Dental Anomalies in Athletes in Qatar: A Panoramic Radiographic Study

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, Dania Almasri, Karim Chamari, Montassar Tabben, Noof AlMabrd, Mohammed Alsaey, Hannah Wesley   +6 more
wiley   +1 more source

Partial primary anodontia associated with ectodermal dysplasia [PDF]

Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”, Chişinău, Republica MoldovaIntroducere. Anodonția este o formă rară de absență parțială sau totală a dentiției, fiind mai frecvent asociată în cadrul unor sindroame genetice, precum ...
Patranac, Maria, Globa, Mihai
core   +1 more source

De Novo Missense Variant in TP63 Gene: Insights on Clinical and Molecular Investigations

The Journal of Gene Medicine, Volume 27, Issue 11, November 2025.
We report a heterozygous missense variant (c.184G〉C, p.Val62Leu) in exon 2 of the TP63 gene in a male patient with ectodermal dysplasia characterized by hypohidrosis, sparse hair, tooth agenesis, cleft lip/palate, hearing loss, and syndactyly. The variant was absent from public databases and unaffected relatives.
Jilong Chen, Xufeng Xi, Xiaoman Xu, Yao Lin   +3 more
wiley   +1 more source