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Genetic Autosomal Dominant Disorders: A Knowledge Review / Trastornos Autosómicos Dominantes: Una Revisión de los Conocimientos
Nogueira, Brenna Magdalena Lima; Silva, Tayana Nascimento da; Nogueira, Bárbara Catarina Lima; da Silva, Walessa Brasil; Menezes, Silvio Augusto Fernandes de; Menezes, Tatiany Oliveira de Alencar.
  • Nogueira, Brenna Magdalena Lima; Federal University of Pará. School of Dentistry. Belém. BR
  • Silva, Tayana Nascimento da; Federal University of Pará. School of Dentistry. Belém. BR
  • Nogueira, Bárbara Catarina Lima; Federal University of Pará. School of Dentistry. Belém. BR
  • da Silva, Walessa Brasil; Federal University of Pará. School of Dentistry. Belém. BR
  • Menezes, Silvio Augusto Fernandes de; Federal University of Pará. School of Dentistry. Belém. BR
  • Menezes, Tatiany Oliveira de Alencar; Federal University of Pará. School of Dentistry. Belém. BR
Int. j. odontostomatol. (Print) ; 9(1): 153-158, Apr. 2015.
Article in English | LILACS | ID: lil-747492
ABSTRACT
Genetic disorders occur by excess or absence of chromosomal material, and the consequence of these changes is reflected in morphological and physiological changes. Autosomal disorders, which have dominant inheritance, as cleidocranial dysostosis, Craniofacial syndrome Apert, Treacher Collins and Achondroplasia have peculiar and similar characteristics. Because of their implications in the dental field, the aim of this review is to report on dysostoses, through exposure of general clinical factors and highlighting the signs in the oral cavity. Articles were selected from Lilacs, PubMed and Bireme databases, included in the year 2007­2014, and the keywords were cleidocranial dysplasia, craniofacial dysostosis, mandibulofacial dysostosis, dysostosis and oral. Alterations of maxillofacial bones and craniofacial are well documented in the literature, but studies reporting an association between treatment odontologic and dysostoses are scarce. In conclusion, Oral pathological manifestations developed cause difficulty in speech, chewing, breathing, social involvement, and in a general perspective, psychological impairment and physical limitations.
RESUMEN
Las enfermedades genéticas se producen debido a un exceso o ausencia de material cromosómico, y la consecuencia de estos cambios se refleja en los cambios morfológicos y fisiológicos. Trastornos autosómicos dominantes que tienen herencia dominante, como la disostosis cleidocraneal, el síndrome craneofacial de Apert, Treacher Collins y acondroplasia tiene características peculiares y similares. Debido a sus implicaciones en el campo de la odontología, el objetivo de esta revisión es hablar, a través de la exposición de los factores clínicos y generales, destacando los signos en la cavidad oral. Se seleccionaron los artículos de las bases de datos Lilacs, PubMed y BIREME, incluyendo los años 2007-2014, y las palabras clave fueron displasia cleidocraneal, craneofacial mandibulofacial disostosis, disostosis y oral. Los cambios de huesos maxilofaciales y craneofaciales están bien documentados en la literatura, pero los estudios que informaron una asociación entre el tratamiento dental y disostosis son escasos. En conclusion, las manifestaciones orales son causas de dificultades del habla, masticación, respiración y la participación social.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Cleidocranial Dysplasia / Craniofacial Dysostosis Type of study: Systematic reviews Limits: Humans Language: English Journal: Int. j. odontostomatol. (Print) Journal subject: Dentistry Year: 2015 Type: Article Affiliation country: Brazil Institution/Affiliation country: Federal University of Pará/BR

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Full text: Available Index: LILACS (Americas) Main subject: Cleidocranial Dysplasia / Craniofacial Dysostosis Type of study: Systematic reviews Limits: Humans Language: English Journal: Int. j. odontostomatol. (Print) Journal subject: Dentistry Year: 2015 Type: Article Affiliation country: Brazil Institution/Affiliation country: Federal University of Pará/BR