Síndrome de gorlin goltz – reporte de caso

Autor: Jardim, Virgílio Bernardino Ferraz, Barros, Allan Vinícius Martins de, Araújo, Rafaella Amorim Bittencourt Maranhão de, Ramos, Lucas Viana Silva, Lima, Luiz Fernando Alves de, Silva, Emanuel Dias de Oliveira e

Publikováno v: Research, Society and Development; Vol. 10 No. 2; e49610210476
Research, Society and Development; Vol. 10 Núm. 2; e49610210476
Research, Society and Development; v. 10 n. 2; e49610210476
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI

Introduction: Gorlin-Goltz syndrome is also referred to as basal cell nevus syndrome or basal cell nevoid carcinoma syndrome. This is a rare autosomal dominant inherited disorder caused by mutation in the PTCH1 tumor suppressor gene. Case report: A 1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3056::0495e69887eef9e92042520a77f34d02
https://rsdjournal.org/index.php/rsd/article/view/10476

SEGMENTAL RESECTION OF THE MANDIBLE FOR THE TREATMENT OF DESMOPLASTIC AMELOBLASTOMA: A CASE STUDY

Autor: ARAÚJO, RAFAELLA AMORIM BITTENCOURT MARANHÃO DE, GOUVEIA, MARCIA MARIA DE, ALVES, CARLOS AUGUSTO FERREIRA, JÚNIOR, PAULO DOMINGOS RIBEIRO, FILHO, JOSÉ ZENOU COSTA, SANTOS, ÍCARO GUILHERME PEREIRA, COSTA, PEDRO JORGE CAVALCANTE

Publikováno v: In Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology September 2020 130(3):e132-e132