Results 51 to 60 of about 628 (133)
Clinical Case Reports, Volume 14, Issue 4, April 2026.ABSTRACT Hypohidrotic ectodermal dysplasia (HED) is a rare congenital disorder characterized by abnormal development of ectodermal structures including hair, teeth, nails, and sweat glands. Dental manifestations such as anodontia or hypodontia can significantly impair mastication, speech development, facial esthetics, and psychosocial well‐being ...
Nazera Ahmadzai +5 more
wiley +1 more source
Esthetic rehabilitation of non-syndromic oligodontia: An innovative approach
Journal of Advanced Clinical & Research Insights, 2015 This case report describes the esthetic rehabilitation of a 13-year-old girl presenting with non-syndromic oligodontia, who had compromised esthetics, occlusal function, development, and retarded skeletal growth. The esthetic rehabilitation was completed with direct composite restoration using thermoformed templates along with reinforced polyethylene ...
P. Poornima +3 more
openaire +1 more source
Orthodontics &Craniofacial Research, Volume 29, Issue 1, Page 1-11, February 2026.ABSTRACT Crouzon and Apert syndromes are rare syndromic craniosynostoses frequently associated with craniofacial and dental anomalies, including tooth agenesis. Although individual studies have reported tooth agenesis prevalence data in specific populations, no attempts have been made to systematically synthesise these data.
M. Cecilia Becerril Santos +3 more
wiley +1 more source
Combined Mutations of LTBP3 and COL5A1A in Geleophysic Dysplasia
Case Reports in Medicine, Volume 2026, Issue 1, 2026.Geleophysic dysplasias (GDs) are uncommon genetically predisposed abnormalities that interfere with skeletal growth and formation. Several GD subtypes have different clinical manifestations. The current report presents the case of a 7‐year‐old Syrian boy with a medical history of repeated bone fractures and noticeable facial characteristics.
Adel Alsharei +10 more
wiley +1 more source
A non-syndromic hereditary oligodontia-a rare case report
Journal of Oral Medicine, Oral Surgery, Oral Pathology and Oral Radiology, 2016 Tooth agenesis is a condition where teeth are missing due to developmental failure. It is often seen in one-quarter of general population making it the most common of human developmental anomalies and it may or may not be associated with syndromes. Oligodontia is a rare hereditary or developmental anomaly showing absence of 6 or more teeth with the ...
Raj Rathore +4 more
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Case Reports in Dentistry, Volume 2026, Issue 1, 2026.Understanding the anatomical variations between primary and permanent dentitions and familiarity with the internal and external root morphology are essential for dental practitioners to distinguish root morphological anomalies. A search in dental literature reveals the occurrence of monoradicular molars in primary dentition; especially the ...
Basim Almulhim, Hannah Wesley
wiley +1 more source
Non-syndromic oligodontia: a case report.
West African journal of medicine, 2011 oligodontia is a condition with developmental absence of six or more permanent teeth excluding the third molars. It is a rare finding which has not been frequently documented in Nigerian children.to report a case of non syndromic oligodontia.The details of the clinical presentation, course and outcome of a 9-year-old child with oligodontia were ...
O O, Bankole, O I, Iyun, O O, Dosunmu
openaire +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
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 +3 more
wiley +1 more source
Expanding the SIAH1‐Associated Phenotypic Spectrum: Insights From Loss‐of‐Function Variants
American Journal of Medical Genetics Part A, Volume 197, Issue 8, August 2025.ABSTRACT SIAH1 encodes for a RING‐type E3 ubiquitin ligase involved in protein ubiquitination. More specifically, it positively regulates Wnt signaling through promoting the accumulation of β‐catenin and mediates ubiquitination and degradation of Akt3 in neural development.
Liza Douiev +14 more
wiley +1 more source