Título: 3C SYNDROME WITH A PREDOMINANCE OF FACIAL CHANGES: A CASE REPORT
Nome do Apresentador: Camila Yasmin Craveiro SACRAMENTO
Categoria do Trabalho: Painel de caso clínico (PCC)
Área Temática: Odontologia para pacientes especiais
Resumo: A rare case of 3C syndrome (craniofacial features, cerebellar defects, and cardiovascular malformations) was diagnosed in a university hospital in northern Brazil. The 3-year-old male patient with delayed neuropsychomotor development and genetic craniofacial dysmorphism (trigonocephaly and high nasal bridge) was referred to the dental clinic. The anamnesis revealed a history of neonatal deaths associated with the autosomal recessive condition. The intraoral examination indicated incompetent lip seal, maxillary atresia, short lingual frenulum (ankyloglossia), limited mouth opening, poor oral hygiene, brown spots on teeth, deciduous teeth, and carious lesions. Frenectomy, tooth extractions (74, 75, 61), and tooth restorations with composite resin and glass ionomer cement were performed; in addition, the patient was guided for adequate oral hygiene and is currently under genetic and dental follow-up.
Autor 1: Camila Yasmin Craveiro SACRAMENTO
E-mail 1: [email protected]
Autor 2: Sandiele Duarte DIAS
E-mail 2: [email protected]
Autor 3 : Isabella Monteiro de MORAES
E-mail 3: [email protected]
Autor 4: Plinio Alves VIEIRA
E-mail 4: [email protected]
Autor 5: Erick Nelo PEDREIRA
E-mail 5: [email protected]
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