Results 21 to 30 of about 3,257 (209)
Primary double tooth with partial anodontia of permanent dentition: a case report [PDF]
, 2010 Dental anomalies of number and forms may occur in the primary and permanent dentition. Various terms have been used to describe dental twinning anomalies: gemination, fusion, concrescence, double teeth, cojoined teeth, twinned teeth ...
Krishnakumar, R. +5 more
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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
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. +6 more
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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 +12 more
doaj +1 more source
Dental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature. [PDF]
Pediatr DermatolABSTRACT We describe a 1‐day old female with features of keratitis‐ichthyosis‐deafness (KID) syndrome and natal teeth. Genetic analysis confirmed GJB2 263C and A88V de novo pathogenic variants consistent with KID syndrome. Natal teeth were promptly extracted to avoid the risk of aspiration.
Maarouf S, Clark M, Chen A, Haggstrom A.
europepmc +2 more sources
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 +5 more
doaj +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
Prevalence of Talon cusp in Indian population [PDF]
, 2012 Aim: To investigate the prevalence of the talon cusps in a sample of Indian dental patients and their distribution among different types of teeth. To determine the presence of other dental anomalies associated with the talon cusps.
Chatra, Laxmikanth +5 more
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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
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