Solitary median maxillary central incisor syndrome
2006
Solitary Median Maxillary Central Incisor Syndrome
publication
Evidence: moderate
Author Information
Author(s): Hall Roger K
Primary Institution: Royal Children's Hospital, Australia
Hypothesis
The study investigates the characteristics and implications of Solitary Median Maxillary Central Incisor (SMMCI) syndrome.
Conclusion
SMMCI syndrome is a complex disorder with various associated congenital anomalies, primarily affecting midline structures.
Supporting Evidence
- SMMCI occurs in approximately 1 in 50,000 live births.
- Congenital nasal malformations are commonly associated with SMMCI.
- Diagnosis can be made as early as 18-22 weeks gestation via ultrasound.
Takeaway
SMMCI syndrome means a child has only one central tooth in the middle of their upper jaw, which can be linked to other health issues.
Methodology
The study reviews existing literature and clinical cases related to SMMCI syndrome.
Limitations
The variability in phenotypic expression and the uncertainty of the syndrome's etiology complicate diagnosis and management.
Digital Object Identifier (DOI)
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