Results 41 to 50 of about 4,843 (273)

NUMERIC DENTAL ANOMALIES IN CHILDREN FROM CLUJ-NAPOCA [PDF]

Romanian Journal of Stomatology, 2018
Numeric tooth anomalies involving a fewer number of teeth (hypodontia) are considered dental dystrophies determined by disturbances during the odontogenesis stage.
Viorica Ţărmure, Radu Septimiu Câmpian, Victor Suciu, Ecaterina Ionescu, Elina Teodorescu, Ştefan Milicescu, Paula Jiman, Olimpia Bunta, Andreea Pop   +8 more
doaj   +1 more source

Novel mutations identified in the WNT10A gene and implant rehabilitation of patients with severe tooth agenesis

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, YU Kang, ZHOU Mengqi, WU Yiqun, WANG Feng   +4 more
doaj   +1 more source

Prosthetic Rehabilitation of a Three-year-old Child with Ectodermal Dysplasia: A Case Report [PDF]

Journal of Clinical and Diagnostic Research
Ectodermal 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, Brahmananda Dutta, S Bhuvaneshwari, Varsha Sharma   +3 more
doaj   +1 more source

Prosthodontic management of hypohidrotic ectodermal dysplasia: a case report [PDF]

, 2015
Introduction: Ectodermal dysplasia (ED) is a hereditary disorder associated with developmental disorders of two or more structures of ectodermal embryonic origin.
Bajraktarova, B., Emilija Bajraktarova Valjakova, Gigovski, N., Guguvcevski, Lj., Korunoska Stevkovska, V., Misevska, C., Sotirovska Ivkovska, A.   +6 more
core   +3 more sources

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, Aparna Sivaraman, CR Sangeetha, Reshma Aloysius, K Risana, Swetha S Nair   +5 more
doaj   +1 more source

PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China

Journal of Applied Oral Science, 2013
Our research aimed to look into the clinical traits and genetic mutations in sporadic non-syndromic anodontia and to gain insight into the role of mutations of PAX9, MSX1, AXIN2 and EDA in anodontia phenotypes, especially for the PAX9.
Jing WANG, Yuanzhi XU, Jing CHEN, Feiyu WANG, Renhuan HUANG, Songtao WU, Linjing SHU, Jingyi QIU, Zhi YANG, Junjie XUE, Raorao WANG, Jilin ZHAO, Wenli LAI   +12 more
doaj   +1 more source

The association between Ponticulus Posticus and Dental Agenesis: a retrospective study [PDF]

, 2018
OBJECTIVE: Neural tube defects may increase the risk of an abnormal development of skull, vertebral column and teeth formation, including dental agenesis in non syndromic patients. The association between the presence of a congenital Dental Agenesis (DA)
Barbato, Ersilia, Galluccio, Gabriella, Leonardi, Rosa Maria, Putrino, Alessandra   +3 more
core   +1 more source

Hypohidrotic ectodermal dysplasia with anodontia: A rare case-rehabilitation by prosthetic management

Journal of Indian Academy of Oral Medicine and Radiology, 2012
Ectodermal dysplasia is a hereditary disorder characterized by developmental dystrophies of ectodermal derivatives- It is characterized by triad of signs comprising sparse hair, abnormal or missing teeth and inability to sweat.
M Naveen Kumar, P Srinivas, S Ramadevi, S Raghavendra Prasad, P Ajayprakash, M Sudhakar   +5 more
doaj   +1 more source

Solitary median maxillary central incisor in association with hemifacial microsomia: A rare case report and review of literature

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, Syed Naved Zahid, Richa Gupta   +2 more
doaj   +1 more source

Sanjad-Sakati Syndrome Dental Management: A Case Report [PDF]

, 2013
Sanjad-Sakati syndrome (SSS) is a rare genetic disorder with autosomal recessive pattern of inheritance characterized by hypoparathyroidism, sever growth failure, mental retardation, susceptibility to chest infection, and dentofacial anomalies.
Hisham Y. El Batawi
core   +1 more source