Dental treatment in a patient with Cornelia de Lange Syndrome: case report

Cornelia de Lange syndrome (CLS) is a rare genetic disease with an estimated prevalence of 1 in every 30,000 live births. The main features are distinct craniofacial disorders, abnormalities in the upper and lower limbs and intellectual deficit, varying between patients, being the main clinical diag...

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Bibliographic Details
Main Author: Gomes, Luana Ferreira (author)
Other Authors: Oliveira, Beatriz Reis de (author), Lima, Naynne Soares de (author), Oliveira, Victória Rocha de (author), Santana, Ellen Maiany Ribeiro (author), Vasconcellos, Sara Juliana de Abreu de (author), Barros, Alina Lúcia de Oliveira (author), Macedo, Álvaro Bezerra (author)
Format: article
Language:por
Published: 2021
Subjects:
Craniofacial Abnormalities
Cornelia de Lange syndrome
Pathology.
Síndrome de Cornelia de Lange
Anomalías Craneofaciales
Patologia.
Anormalidades Craniofaciais
Online Access:https://doi.org/10.33448/rsd-v10i11.19531
Country:Brazil
Oai:oai:ojs.pkp.sfu.ca:article/19531

Internet

https://doi.org/10.33448/rsd-v10i11.19531

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