Results 31 to 40 of about 2,260 (205)
Primary Teeth Supported Fixed Prosthesis—A Predictable Treatment Alternative
Children, 2022 Background: Individuals with tooth agenesis often present a significant clinical challenge for dental practitioners. This retrospective study evaluated clinical and radiological long-term functional and esthetic outcomes following restoration using ...
Sarit Naishlos +8 more
doaj +1 more source
, 2007 Genus Anodontia Link, 1807 Anodontia Link, 1807: 156. TYPE SPECIES. — A. alba Link, 1807 (monotypy). DIAGNOSIS. — Shells small to large, relatively thin-shelled, usually white, globose, subcircular, exterior smooth with irregular commarginal ...
Glover, Emily A., Taylor, John D.
core +1 more source
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
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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
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
Molecular Basis and Clinical Spectrum of WNT10A‐Related Oligodontia
Clinical Genetics, Volume 110, Issue 1, Page 3-14, July 2026.Cellular Mechanism behind WNT10A phenotypes. ABSTRACT WNT10A mutations, a major genetic determinant of dental agenesis and ectodermal dysplasia, exert profound effects on craniofacial development. Although classified as rare disorders, these mutations account for more than half of oligodontia cases, reflecting their critical role.
Perennes Elise +5 more
wiley +1 more source
, 2006 Genus Anodontia Link, 1807 TYPE SPECIES. — Anodontia alba Link, 1807, by original designation. SPECIES INCLUDED. — 25 species (Taylor & Glover 2005), worldwide. DIAGNOSIS. — Shells small to very large, equivalve, inequilateral, very tumid to globose,
Cosel, Rudo von
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Environmental DNA, Volume 8, Issue 3, May–June 2026.This review reveals major genetic data gaps for Philippine mangrove fauna, especially invertebrates, limiting species‐level eDNA detection. By compiling 48 years of biodiversity records and assessing reference library coverage, it highlights the need for targeted sequencing and shows how integrating eDNA with conventional surveys strengthens monitoring
Earl Kevin T. Cooper +14 more
wiley +1 more source
The Journal of Indian Prosthodontic Society, 2022 Treatment of pediatric patients with partial anodontia is a challenge requiring interdisciplinary approach. Growth period, reduced vertical dimension, microdontia, and unacceptable esthetics present difficulties at various stages of prosthetic ...
Natarajan Kalavathy +4 more
doaj +1 more source
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