Orofacial findings and dental care management in a patient with Robinow Syndrome

Autor: Marina Fernandes de Sena, Thais Tedeschi dos Santos, Karina Mayra de Queiroz Brito, Alexandra Mussolino de Queiroz, Carolina Paes Torres, Francisco Wanderley Garcia Paula-Silva, Fábio Lourenço Romano, Sandra Maria Garcia da Silveira, Paôla Caroline da Silva Mira

Publikováno v: Revista Científica do CRO-RJ (Rio de Janeiro Dental Journal); Vol. 4 No. 2: May-August 2019; 60-66
Revista Científica do CRO-RJ (Rio de Janeiro Dental Journal); v. 4 n. 2: May-August 2019; 60-66
Revista Científica do CRO-RJ
Conselho Regional de Odontologia do Rio de Janeiro (CRO-RJ)
instacron:CRO

Introduction: Robinow syndrome is a rare genetic disorder of skeletal development. It is characterized by short stature, facial dysmorphisms and orodental anomalies, underdeveloped genitalia, mesomelic brachymelia. Case Report: A 6 year old girl with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::797780106955fbf7b713d6d1ed004103
https://doi.org/10.29327/24816.4.2-11