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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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| Publicado no: | Appl Clin Genet |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8179788/ https://ncbi.nlm.nih.gov/pubmed/34103968 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S280066 |
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