Zobrazeno 1 - 10
of 51
pro vyhledávání: '"tooth malformation"'
Autor:
Yang Haoqing, Fan Zhipeng
Publikováno v:
生物医学转化, Vol 4, Iss 3, Pp 47-56 (2023)
Congenital tooth developmental anomalies refer to a type of tooth disease where the shape or structure of the teeth is abnormal during embryonic development or after birth. Such anomalies may affect the growth, chewing function, and aesthetics of the
Externí odkaz:
https://doaj.org/article/23108f55808f4718b17a6c75a955c6e6
Publikováno v:
Dental Hypotheses, Vol 6, Iss 3, Pp 117-122 (2015)
Introduction: Maxillary sinusitis can have various origins, including odontogenic origin. Case Report: We describe a case of maxillary sinusitis in a 25-year-old female patient who experienced pain and swelling in the right maxillary region as a comp
Externí odkaz:
https://doaj.org/article/1fa9440e2c3e4962b5810060e504ff18
Autor:
Pratima Shenoi, Manjusha S Pradhan, Vidya Mokhade, Varsha Uttarwar, Rajesh Kubde, Chetana S Makade, Mohit Gunwal
Publikováno v:
IP Indian Journal of Conservative and Endodontics. 5:1-3
Dental fluorosis (DF) is a tooth malformation related to ingestion of high amount of fluoride (F) during tooth development. According to various surveys (1994 , 2000 & 2002), it is clearly established that DF has increased incidences rates in the are
Autor:
Sara A Rodríguez-Aguirre, Juan P Gómez, Flora M Campos, Angela María Duque, Sara Gómez-Arango, Javier Eslava-Schmalbach, Sandra L Posso-Moreno, Liliana Otero, Salomón Yezioro-Rubinsky, Nathaly Garzón-Orjuela, Nancy Edith Rojas
Publikováno v:
The Cleft Palate-Craniofacial Journal. 57:73-79
Objectives: To assess the risk of dental anomaly presentation in permanent teeth in a group of Colombian children with nonsyndromic cleft lip and palate (NSCLP) and to determine the frequency of the anomalies according to the cleft type. Methods: An
Autor:
Badran, Zahi, Lopez-Cazaux, Serena, Crauste, Eleonore, Bray, Estelle, Soueidan, Assem, Armengol, Valérie, Di Donato, N., Isidor, B., Lopez Cazaux, S., Le Caignec, C., Klink, B., Kraus, C., Schrock, E., Hackmann, K.
Publikováno v:
European Journal of Dentistry
European Journal of Dentistry, 2019, 10 (04), pp.579-582. ⟨10.4103/1305-7456.195167⟩
European Journal of Dentistry, Thieme, 2016, 10 (4), pp.579-582. ⟨10.4103/1305-7456.195167⟩
European Journal of Dentistry, Thieme, 2019, 10 (04), pp.579-582. ⟨10.4103/1305-7456.195167⟩
European Journal of Dentistry, 2019, 10 (04), pp.579-582. ⟨10.4103/1305-7456.195167⟩
European Journal of Dentistry, Thieme, 2016, 10 (4), pp.579-582. ⟨10.4103/1305-7456.195167⟩
European Journal of Dentistry, Thieme, 2019, 10 (04), pp.579-582. ⟨10.4103/1305-7456.195167⟩
Dental invagination (DI) is a tooth malformation that usually affects permanent teeth. Its precise etiology is still controversial and represents a clinical challenge as it can favor the development of carious lesion or periodontal inflammation. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70a617bb47bd1bb95612c524f042ba47
https://hal.archives-ouvertes.fr/hal-02517081
https://hal.archives-ouvertes.fr/hal-02517081
Publikováno v:
Contemporary Clinical Dentistry, Vol 1, Iss 1, Pp 45-46 (2010)
Most supernumerary impacted teeth are located in the anterior maxillary region. They are classified according to their form and location. Their presence may give rise to a variety of clinical problems. The detection of supernumerary teeth is best ach
Externí odkaz:
https://doaj.org/article/71de1953251e4760b3972361e17b29c1
Publikováno v:
Current Stem Cell Research & Therapy. 13
Background Odontogenesis is fundamentally controlled by the genome. However, epigenetic factors have indispensable effects during odontogenesis. Previous studies have shown that exogenous factors, such as the environment, that cause hypomethylation a
Akademický článek
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Publikováno v:
Revista Cubana de Estomatología, Vol 42, Iss 1, p 0 (2005)
La displasia ectodérmica es una enfermedad genética muy rara, la cual se encuentra caracterizada por manifestaciones odontoestomatológicas imponentes; presenta aspectos interesantes desde el punto de vista del diagnóstico, así como la rehabilita
Externí odkaz:
https://doaj.org/article/ddefaf8117de4f0285c677ce12e284e2
Publikováno v:
Dokkyo journal of medical sciences. 39(2):119-122
Joubert syndrome-related disorders (JSRD) is a very rare syndrome observed with agenesis of the vermis,episodic hyperpnea, abnormal eye movements, and cerebellar ataxia and mental retardation. There have been many reports on the image-based diagnosis