Results 21 to 30 of about 4,786 (283)

The two extremes of physiological tooth resorption in primary tooth with or without the permanent successor tooth

Dental Press Journal of Orthodontics, 2021
Introduction: Assessment of two radiographic images reveals two distinct, extreme situations of physiological tooth resorption, characteristic of primary teeth with or without permanent successor, due to partial anodontia.
Alberto CONSOLARO, Moacyr Tadeu RODRIGUES, Renata Bianco CONSOLARO, Giovana Gonçalves MARTINS   +3 more
doaj   +1 more source

Anodontia de dentes permanentes: uma revisão integrativa

Brazilian Journal of Development, 2023
Entende-se por agenesia o decréscimo em número dentário de um ou mais elementos. Ou seja, consiste na ausência de dentes seja na dentição decídua ou permanente.
Áyla Geovânia da Silva Peixoto, Franklin Flamarion Gomes Peixoto, Dannyellen Maria de Siqueira Gomes Taveiros, Juliana Vilela Ribeiro De Souza   +3 more
semanticscholar   +1 more source

DCAF17 Mutation in Woodhouse-Sakati Syndrome: A Case Report on a Novel Homozygous Variant. [PDF]

Case Rep Pediatr
Background: Woodhouse–Sakati syndrome (WSS) is a rare autosomal recessive disorder characterized by a constellation of symptoms, including alopecia, hypogonadism, diabetes, mental retardation, and extrapyramidal syndrome. Here, we present a case study of a girl with WSS, focusing on clinical features, genetic analysis, and treatment.
Khalili Dehkordi A, Vakili R.
europepmc   +2 more sources

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

Various aspects of two treatment approaches to patients with problems of hypodontia of upper lateral incisors [PDF]

Vojnosanitetski Pregled, 2021
Introduction. The treatment of hypodontia of the upper lateral incisors could be orthodontic or multidisciplinary with combined orthodontic, surgical and prosthetic involvement. Both options have their pros and cons.
Stojanović Ljiljana, Galluccio Gabriella, Todorović Aleksandar, Zoran Lazić, Tsolakis Apostolos, Pajević Tina   +5 more
doaj   +1 more source

X-linked hypohidrotic ectodermal dysplasia management with removable prosthesis in a pediatric patient. Case Report.

Journal of Oral Research, 2022
Introduction: Ectodermal dysplasia is a rare genetic disorder that affects structures derived from ectoderm such as teeth, hair, nails, and sweat glands.
Héctor Rodríguez, José Rodríguez, Maria Acosta de Camargo, Hazel Topel, Miguel Hirschhaut   +4 more
doaj   +1 more source

Hypohidrotic Ectodermal Dysplasia with total anodontia: a case report [PDF]

, 2011
Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ectoderm of the developing embryo. The triad of nail dystrophy, alopecia or hypotrichosis and palmoplantar hyperkeratosis is usually accompanied by a lack ...
Sathyajith Naik, N., Shashibhushan, K.K., Subba Reddy, V.V., Viswanathan, Revathy   +3 more
core   +1 more source

Radiographic evaluation of the prevalence of dental anomalies of number [PDF]

Revista Portuguesa de Estomatologia, Medicina Dentária e Cirurgia Maxilofacial, 2023
Objectives: This study aims to determine the prevalence of tooth agenesis and supernumerary teeth and characterize both anomalies in a Portuguese pediatric population.
Gonçalo D. Costa, Pedro Mesquita
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

New observation of severe tooth malformation in a female patient with ectodermal dysplasia due to the EDA splice acceptor variant c.742‐2A>G

Molecular Genetics &Genomic Medicine, Volume 11, Issue 12, December 2023., 2023
Our study points that the very rare splice acceptor variant EDA c.742‐2A>G associates with severe oligodontia and is pathogenic. Abstract Background Ectodermal dysplasias are inherited disorders, which are characterized by congenital defects in two or more ectodermal structures such as skin, sweat glands, hair, nails, teeth, and mucous membranes ...
Vivian Reinhold, Stina Syrjänen, Minna Kankuri‐Tammilehto   +2 more
wiley   +1 more source