The Oral Health of Patients with DiGeorge Syndrome (22q11) Microdeletion: A Case Report

BACKGROUND: DiGeorge syndrome (DG) is a genetic disorder associated with 22q11 deletion. It involves various phenotypes, including craniofacial abnormalities, congenital heart disorders, endocrine dysfunction, cognitive deficits, and psychiatric disorders. Cases commonly involve multiple anomalies....

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Detalles Bibliográficos
Autores principales: Candelo, Estephania, Estrada-Mesa, Maria Alejandra, Jaramillo, Adriana, Martinez-Cajas, Carlos Humberto, Osorio, Julio Cesar, Pachajoa, Harry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179788/
https://www.ncbi.nlm.nih.gov/pubmed/34103968
http://dx.doi.org/10.2147/TACG.S280066

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179788/
https://www.ncbi.nlm.nih.gov/pubmed/34103968
http://dx.doi.org/10.2147/TACG.S280066

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