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- Title
SATB2-associated syndrome: a case report.
- Authors
Issad, Mehdi; Ahossi, Victorin; Melli, Emma; Hoarau, David
- Abstract
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.
- Subjects
ORAL hygiene; CORRECTIVE orthodontics; SPEECH therapy; SYNDROMES; FACIAL abnormalities
- Publication
Journal of Oral Medicine & Oral Surgery, 2024, Vol 30, Issue 1, p1
- ISSN
2608-1326
- Publication type
Article
- DOI
10.1051/mbcb/2024003