Results 21 to 30 of about 2,260 (205)
口腔疾病防治, 2022 Objective To detect WNT10A gene mutations in patients with oligodontia or anodontia (≥6 teeth missing) and analyze their dental phenotype. Methods Patients with oligodontia or anodontia were enrolled from the clinic for oral examination, genetic history ...
JIANG Xinke +4 more
doaj +1 more source
Prevalence and Patterns of Permanent Tooth Agenesis in Patients With Crouzon or Apert Syndrome: A Systematic Review and Meta-Analysis. [PDF]
Orthod Craniofac ResABSTRACT 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.
Becerril Santos MC +3 more
europepmc +2 more sources
Anodontia - A Case Report [PDF]
, 2015 A case of partial anodontia has been presented. The Physical andclinical examination have been reviewed and the management of the condition has been ...
Bakilana, P
core +1 more source
Prosthetic Rehabilitation of a Three-year-old Child with Ectodermal Dysplasia: A Case Report [PDF]
Journal of Clinical and Diagnostic ResearchEctodermal Dysplasia (ED) is a rare congenital syndrome that exhibits defects in two or more ectodermal tissues. Dental manifestations include delayed eruption of permanent dentition, complete absence of teeth or absence of a few teeth, and peg-shaped ...
Yashshwini Shroff +3 more
doaj +1 more source
Full Mouth Rehabilitation of an Adolescent Patient with Ectodermal Dysplasia: A Case Report [PDF]
Journal of South Asian Association of Pediatric Dentistry, 2022 Ectodermal dysplasia comprises genetic disorders of divergent groups that include dystrophies of ectodermally derived structures and their accessory structures, including hair, glands, teeth, skin, and nails.
Amith Adyanthaya +5 more
doaj +1 more source
Ectodermal Dysplasia with Partial Anodontia: A Case Report and Review [PDF]
, 2019 Ectodermal dysplasia is an X-Linked, recessive hereditary disease characterized by dysplasia of tissues of ectodermal origin. In Hypohidrotic Ectodermal Dysplasia (HED) males are more affected than female .The incidence of ectodermal dysplasia is rare (1
Tarun Vyas, Satish Bhosale
core +1 more source
Step Wise Management of Asyndromic Tooth Agenesis with Ankyloglossia: A Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2021 Ankyloglossia or tongue tie refers to restricted tongue movements, diagnosed in early childhood and adolescence that may cause changes in bone growth and other orofacial tissues results in altered oral functions of the child.
Vandana R Gadve, Vijaya S Dhote
doaj +1 more source
Contemporary Clinical Dentistry, 2011 Solitary median maxillary central incisor (SMMCI) is a rare dental anomaly. It is estimated to occur in 1:50,000 live births. The SMMCI tooth differs from the normal central incisor in that the crown form is symmetric and it develops and erupts precisely
Ashok Utreja +2 more
doaj +1 more source
X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle
Genetics Selection Evolution, 2003 Ectodermal dysplasias are a large group of rare genetic disorders characterized by impaired development of hair, teeth, and eccrine glands in humans, mice, and cattle.
Drögemüller Cord +2 more
doaj +1 more source
Prosthetic rehabilitation of a young patient with Hypophosphatasia - A review and case report
Contemporary Clinical Dentistry, 2012 Hypophosphatasia is a congenital disease characterized by deficiency of serum and tissue non-specific alkaline phosphatase activity. The disease occurs due to mutations in the liver/bone/kidney alkaline phosphatase gene.
Partapjot S Grewal, Kanu Priya Gupta
doaj +1 more source