Relevant bibliographies by topics / Cleidocranial dysplasia review

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Cleidocranial dysplasia review'

Author: Grafiati
Published: 4 September 2021
Last updated: 29 July 2025

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Journal articles on the topic "Cleidocranial dysplasia review"

1

Puvabanditsin, Surasak, Melissa February, Julia Mayne, Jennifer McConnell, and Rajeev Mehta. "Cleidocranial Dysplasia with 6p21.1-p12.3 Microdeletion." Cleft Palate-Craniofacial Journal 55, no. 6 (2018): 891–94. http://dx.doi.org/10.1597/15-306.

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Objective: The aim of this article is to publish a literature review and report on a new case of cleidocranial dysplasia syndrome with 6p21.1-p12.3 microdeletion. Design: A PubMed search using “cleidocranial dysplasia syndrome (CCD)” or “6p microdeletion” was performed. Articles with information relevant to our case were obtained for review. A new case of cleidocranial dysplasia syndrome is presented to describe and discuss clinical manifestations, pathogenesis, clinical progression of cleidocranial dysplasia syndrome, and management. Results: There were 22 articles with reports of cleidocrani
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2

Teslenco, Vítor Bruno, Maylson Alves Nogueira Barros, Everton Floriano Pancini, Herbert de Abreu Cavalcanti, and Guilherme Nucci dos Reis. "Hiperdontia em paciente portadora de displasia cleidocraniana, acompanhamento de 14 anos: relato de caso." ARCHIVES OF HEALTH INVESTIGATION 9, no. 6 (2020): 553–56. http://dx.doi.org/10.21270/archi.v9i6.4774.

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Introdução: Anomalias de forma, tamanho, formato, número, estrutura, e erupção dentária são comumente vistas dentro da odontologia. Dentre elas temos a hiperdontia ou dentes suprenumerários. A etiologia desta patologia não foi realmente esclarecida, porém estas anormalidades são gerenciadas por um complexo sistema de interação genética e ambiental. Objetivo: relatar à comunidade científica um caso diagnosticado como displasia cleidocraniana, onde foram removidos 34 dentes supranumerários de uma paciente. Relato de caso: Paciente do gênero feminino, 12 anos de idade, diagnosticada com displasia
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3

Alfadil, Lina, Paras Jiteshkumar Haria, Priya Haria, et al. "A review of the dental management of cleidocranial dysplasia." Orthodontic Update 18, no. 1 (2025): 33–44. https://doi.org/10.12968/ortu.2025.18.1.33.

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Cleidocranial dysplasia, linked to a mutation in the RUNX2 gene, is characterized by defective endochondral and intra-membranous bone formation. General features include a combination of aplasia or hypoplasia of one or both clavicles, a short skull, delayed ossification of the fontanelles and short stature. Dental anomalies include delayed exfoliation of primary teeth, multiple supernumerary teeth and multiple impacted teeth. The dental management of such cases is complicated. This review summarizes the multiple treatment strategies for the dental management of cleidocranial dysplasia. Combine
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Mabrouk, Yosra, Sinda Ammar, Amel Labidi, Lamia Mansour, and Sonia Ghoul. "Dental Prosthetic Treatments in Cleidocranial Dysplasia: Case Report and Literature Review." Case Reports in Dentistry 2020 (December 19, 2020): 1–8. http://dx.doi.org/10.1155/2020/8910798.

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Cleidocranial dysplasia (CCD) is a rare inherited skeletal syndrome. There is no consensus regarding the dental treatment strategy. Objectives. To report a rare case of cleidocranial dysplasia and to summarize the current clinical and dental features and prosthetic treatment of similar CCD patients reported in the literature. Results. A 17-year-old girl was diagnosed with CCD. She had a short stature with the ability to bring the shoulders under the chest. All remaining teeth were deciduous except the four first molars were permanent. The maxilla was hypoplastic with a relative prognathism of
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5

Avendaño, Andrea, Francisco Cammarata-Scalisi, Mochamad Fahlevi Rizal, et al. "Cleidocranial dysplasia. A molecular and clinical review." International Dental Research 8, no. 1 (2018): 35–38. http://dx.doi.org/10.5577/intdentres.2018.vol8.no1.6.

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Cleidocranial dysplasia (CCD) is a rare autosomal dominant disorder characterized by skeletal and dental abnormalities primarily, short stature, aplasia or hypoplasia of clavicles, open fontanelles and supernumerary teeth. Heterozygous mutations of the runt related transcription factor 2 (RUNX2) gene have been found in approximately 60-70% of cases leaving a large number of cases with no defined genetic cause which led us to delve into molecular mechanisms underlying CCD and thus to detect potential target genes to be explored in these patients. In this review we also highlight very broadly th
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6

Jayachandran, S., and Virender Gombra. "Cleidocranial dysplasia: Report of 4 cases and review." Journal of Indian Academy of Oral Medicine and Radiology 20, no. 1 (2008): 23. http://dx.doi.org/10.4103/0972-1363.44357.

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7

Perez, Alexandre, Sarah Dib, Andreij Terzic, Delphine Courvoisier, and Paolo Scolozzi. "Survival of dental implants in patients with bone dysplasia: A systematic review." Discussion of Clinical Cases 8, no. 4 (2021): 8. http://dx.doi.org/10.5430/dcc.v8n4p8.

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Objective: This study used published studies to assess the survival rate of dental implants placed in patients with bone dysplasia of the maxillofacial region.Material and methods: An electronic search without a specified date range was performed using the MEDLINE, PubMed, EMBASE, Web of Science, and Cochrane databases. No gender or age restrictions were applied.Results: Eighteen publications were found that met the study’s criteria, reporting data on 18 patients with bone dysplasia including cleidocranial dysplasia (CDD), fibrous dysplasia (FD), florid cemento-osseous dysplasia (FCOD), and od
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8

Prata, Vitória Pigari, Geovanna Maria Ramos Porto De Souza, Luana Ferreira Oliveira, Giselle Juliana De Jesus, Valéria Cristina Lopes de Barros Rolim, and José Antonio Santos Souza. "Displasia cleidocraniana e a odontologia: revisão de literatura / Cleidocranial dysplasia and dentistry: literature review." Brazilian Journal of Health Review 4, no. 6 (2021): 26658–68. http://dx.doi.org/10.34119/bjhrv4n6-242.

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9

Zheng Shen, Chao Chun Zou, Rong Wang Yang, and Zheng Yan Zhao. "Cleidocranial Dysplasia: Report of 3 Cases and Literature Review." Clinical Pediatrics 48, no. 2 (2008): 194–98. http://dx.doi.org/10.1177/0009922808323107.

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10

Jain, Harshika, Akansha Budakoti, Rupali Pandey, Deepankar Misra, and Anish Kumar. "Cleidocranial Dysplasia: A Serendipitous Finding with Clinical Insights." Current Trends in Dentistry 2, no. 1 (2025): 51–54. https://doi.org/10.4103/ctd.ctd_5_25.

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Abstract Cleidocranial dysplasia (CCD) is an uncommon congenital condition that is distinguished by a distinct set of dental and skeletal abnormalities. Together with a clinical evaluation, the imaging results aid in making a conclusive diagnosis. It is crucial to comprehend the wide range of CCD symptoms to manage and treat the condition effectively. With an emphasis on the genetic etiologies, clinical presentation, radiological findings, and a review of recent research, this case report attempts to give a thorough account of a male patient with CCD who is 25 years old. The goal is to raise a
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Dissertations / Theses on the topic "Cleidocranial dysplasia review"

1

Loureiro, Luís Albino Marques. "Displasia cleidocraniana: uma revisão da literatura." Master's thesis, 2015. http://hdl.handle.net/10316/37405.

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