Please use this identifier to cite or link to this item: https://repositorio.ufu.br/handle/123456789/19937
Document type: Trabalho de Conclusão de Curso
Access type: Acesso Embargado
Title: Cases report: cri-du-chat syndrome
Author: Medeiros, jessica brenda rodrigues de
First Advisor: Castro, alessandra maia castro prado
First coorientator: Marques, késia lara dos santos marques
First member of the Committee: Ferreira, danielly cunha araújo ferreira de oliveira
Second member of the Committee: Oliveira, fabiana sodré de oliveira
Third member of the Committee: Georjutti, renata pereira georjutti
Summary: The Cri-du-chat syndrome is an autosomal genetic disorder described by Lejejune in 1963, which involves the partial or total deletion of the chromosome 5 (5p). The syndrome is considered rare, with a prevalence of 1: 15,000 and 1: 50,000, with specific alterations. The aim of this study was to report three clinical cases that involve patients with Cri-du-chat syndrome emphasizing the cranio-skeletal and orofacial characteristics, that may imapair on the dental care. The cranio-skeletal and orofacial alterations in these patients were described and compared on the literature. Pathognomonic characteristics of the Cri-du-chat syndrome were found in the cases described. In one of them a mosaicism karyotype was observed as the cause of deletion chromosome 5. The knowledge of the syndrome’s characteristics, the resultante, systemic and oral problems, allows greater safety when planning and executing the dental treatment.
Abstract: The Cri-du-chat syndrome is an autosomal genetic disorder described by Lejejune in 1963, which involves the partial or total deletion of the chromosome 5 (5p). The syndrome is considered rare, with a prevalence of 1: 15,000 and 1: 50,000, with specific alterations. The aim of this study was to report three clinical cases that involve patients with Cri-du-chat syndrome emphasizing the cranio-skeletal and orofacial characteristics, that may imapair on the dental care. The cranio-skeletal and orofacial alterations in these patients were described and compared on the literature. Pathognomonic characteristics of the Cri-du-chat syndrome were found in the cases described. In one of them a mosaicism karyotype was observed as the cause of deletion chromosome 5. The knowledge of the syndrome’s characteristics, the resultante, systemic and oral problems, allows greater safety when planning and executing the dental treatment.
Notes: possui versão em CD
Keywords: Cri-du-Chat Syndrome
5p deletion syndrome
Orofacial manifestation
Area (s) of CNPq: CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA
Language: eng
Country: Brasil
Publisher: Universidade Federal de Uberlândia
Quote: Medeiros JBR. Cases report: cri-du-chat syndrome. 2017. 32 f. Trabalho de Conclusão de Curso (Graduação em Odontologia) - Universidade Federal de Uberlândia, Uberlândia, 2015.
URI: https://repositorio.ufu.br/handle/123456789/19937
Date of defense: 7-Nov-2017
Appears in Collections:TCC - Odontologia

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