| Issue |
J Oral Med Oral Surg
Volume 30, Number 1, 2024
|
|
|---|---|---|
| Article Number | 1 | |
| Number of page(s) | 5 | |
| DOI | https://doi.org/10.1051/mbcb/2024003 | |
| Published online | 26 February 2024 | |
Case Report
SATB2-associated syndrome: a case report
Department of Odontology and Oral Surgery, Dijon-Bourgogne University Hospital, 14 rue Paul Gaffarel, 21000 Dijon, France
* Correspondence: mehdi.issad@chu-dijon.fr
Received:
23
October
2023
Accepted:
5
January
2024
Introduction: SATB2-associated syndrome is an extremely rare genetic disorder. It is characterized by delayed neurocognitive development, craniofacial anomalies and dental defects. Observation: This case report highlights the craniofacial and dental phenotype linked to a mutation resulting in SATB2-associated syndrome affecting a 13-year-old boy. Conclusion: The diagnosis of this syndrome is very difficult. The management using a multidisciplinary strategy includes among others, oral hygiene maintenance, orthodontic treatment and intensive speech therapy.
Key words: SATB2-associated syndrome (SAS) / glass syndrome / facial dysmorphism / dental anomalies
© The authors, 2024
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