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Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report

Background: Cleidocranial dysplasia (CCD) is a rare, autosomal dominant skeletal dysplasia with a prevalence of one per million births. The main causes of CCD are mutations in the core-binding factor alpha-1 (CBFA1) or runt-related transcription factor-2 (RUNX2), located at the 6p21 chromosomal regi...

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Autores principales: Inchingolo, Alessio Danilo, Patano, Assunta, Coloccia, Giovanni, Ceci, Sabino, Inchingolo, Angelo Michele, Marinelli, Grazia, Malcangi, Giuseppina, Montenegro, Valentina, Laudadio, Claudia, Palmieri, Giulia, Bordea, Ioana Roxana, Ponzi, Emanuela, Orsini, Paola, Ficarella, Romina, Scarano, Antonio, Lorusso, Felice, Dipalma, Gianna, Corsalini, Massimo, Gentile, Mattia, Venere, Daniela Di, Inchingolo, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709258/
https://www.ncbi.nlm.nih.gov/pubmed/34946295
http://dx.doi.org/10.3390/medicina57121350
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author Inchingolo, Alessio Danilo
Patano, Assunta
Coloccia, Giovanni
Ceci, Sabino
Inchingolo, Angelo Michele
Marinelli, Grazia
Malcangi, Giuseppina
Montenegro, Valentina
Laudadio, Claudia
Palmieri, Giulia
Bordea, Ioana Roxana
Ponzi, Emanuela
Orsini, Paola
Ficarella, Romina
Scarano, Antonio
Lorusso, Felice
Dipalma, Gianna
Corsalini, Massimo
Gentile, Mattia
Venere, Daniela Di
Inchingolo, Francesco
author_facet Inchingolo, Alessio Danilo
Patano, Assunta
Coloccia, Giovanni
Ceci, Sabino
Inchingolo, Angelo Michele
Marinelli, Grazia
Malcangi, Giuseppina
Montenegro, Valentina
Laudadio, Claudia
Palmieri, Giulia
Bordea, Ioana Roxana
Ponzi, Emanuela
Orsini, Paola
Ficarella, Romina
Scarano, Antonio
Lorusso, Felice
Dipalma, Gianna
Corsalini, Massimo
Gentile, Mattia
Venere, Daniela Di
Inchingolo, Francesco
author_sort Inchingolo, Alessio Danilo
collection PubMed
description Background: Cleidocranial dysplasia (CCD) is a rare, autosomal dominant skeletal dysplasia with a prevalence of one per million births. The main causes of CCD are mutations in the core-binding factor alpha-1 (CBFA1) or runt-related transcription factor-2 (RUNX2), located at the 6p21 chromosomal region. RUNX2 plays important roles in osteoblast differentiation, chondrocyte proliferation and differentiation, and tooth formation. The disease is characterized by clavicular aplasia or hypoplasia, Wormian bones, delayed closure of cranial suture, brachycephalic head, maxillary deficiency, retention of primary teeth, inclusion of permanent teeth, and multiple supernumerary teeth. Materials and Methods: A 22-year-old girl suffering from cleidocranial dysplasia with short stature, narrow shoulders, craniofacial manifestations (short face, broad forehead, etc.) and dental anomalies (different lower dental elements under eruption, supernumerary and impacted multiple teeth, etc.) was examined at our service (Complex Operative Unit of Odontostomatology of Policlinico of Bari). RX Orthopantomography (OPG) and cone beam computed tomography (CBCT) were requested to better assess the position of the supernumerary teeth and their relationships with others and to evaluate the bone tissue. Results: Under eruption was probably caused by dental interferences with supernumerary teeth; hence, extractions of supernumerary upper canines and lower premolars were performed under general anaesthesia. Surgery outcome was excellent with good tissue healing and improvements in the therapeutic possibilities with future orthodontics. Conclusions: The objective of this article is to give an update about radiological, clinical, and molecular features of CCD and to alert the health team about the importance of establishing an early diagnosis and an appropriate treatment in these patients to prevent impacted teeth complications and to offer them a better quality of life.
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spelling pubmed-87092582021-12-25 Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report Inchingolo, Alessio Danilo Patano, Assunta Coloccia, Giovanni Ceci, Sabino Inchingolo, Angelo Michele Marinelli, Grazia Malcangi, Giuseppina Montenegro, Valentina Laudadio, Claudia Palmieri, Giulia Bordea, Ioana Roxana Ponzi, Emanuela Orsini, Paola Ficarella, Romina Scarano, Antonio Lorusso, Felice Dipalma, Gianna Corsalini, Massimo Gentile, Mattia Venere, Daniela Di Inchingolo, Francesco Medicina (Kaunas) Article Background: Cleidocranial dysplasia (CCD) is a rare, autosomal dominant skeletal dysplasia with a prevalence of one per million births. The main causes of CCD are mutations in the core-binding factor alpha-1 (CBFA1) or runt-related transcription factor-2 (RUNX2), located at the 6p21 chromosomal region. RUNX2 plays important roles in osteoblast differentiation, chondrocyte proliferation and differentiation, and tooth formation. The disease is characterized by clavicular aplasia or hypoplasia, Wormian bones, delayed closure of cranial suture, brachycephalic head, maxillary deficiency, retention of primary teeth, inclusion of permanent teeth, and multiple supernumerary teeth. Materials and Methods: A 22-year-old girl suffering from cleidocranial dysplasia with short stature, narrow shoulders, craniofacial manifestations (short face, broad forehead, etc.) and dental anomalies (different lower dental elements under eruption, supernumerary and impacted multiple teeth, etc.) was examined at our service (Complex Operative Unit of Odontostomatology of Policlinico of Bari). RX Orthopantomography (OPG) and cone beam computed tomography (CBCT) were requested to better assess the position of the supernumerary teeth and their relationships with others and to evaluate the bone tissue. Results: Under eruption was probably caused by dental interferences with supernumerary teeth; hence, extractions of supernumerary upper canines and lower premolars were performed under general anaesthesia. Surgery outcome was excellent with good tissue healing and improvements in the therapeutic possibilities with future orthodontics. Conclusions: The objective of this article is to give an update about radiological, clinical, and molecular features of CCD and to alert the health team about the importance of establishing an early diagnosis and an appropriate treatment in these patients to prevent impacted teeth complications and to offer them a better quality of life. MDPI 2021-12-10 /pmc/articles/PMC8709258/ /pubmed/34946295 http://dx.doi.org/10.3390/medicina57121350 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Inchingolo, Alessio Danilo
Patano, Assunta
Coloccia, Giovanni
Ceci, Sabino
Inchingolo, Angelo Michele
Marinelli, Grazia
Malcangi, Giuseppina
Montenegro, Valentina
Laudadio, Claudia
Palmieri, Giulia
Bordea, Ioana Roxana
Ponzi, Emanuela
Orsini, Paola
Ficarella, Romina
Scarano, Antonio
Lorusso, Felice
Dipalma, Gianna
Corsalini, Massimo
Gentile, Mattia
Venere, Daniela Di
Inchingolo, Francesco
Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report
title Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report
title_full Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report
title_fullStr Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report
title_full_unstemmed Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report
title_short Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report
title_sort genetic pattern, orthodontic and surgical management of multiple supplementary impacted teeth in a rare, cleidocranial dysplasia patient: a case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709258/
https://www.ncbi.nlm.nih.gov/pubmed/34946295
http://dx.doi.org/10.3390/medicina57121350
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