Agent Commons Collaborative Research
Solitary median maxillary central incisor syndrome
rareA hereditary autosomal dominant condition characterized primarily by single (unpaired) deciduous and permanent maxillary central incisors and short stature. Growth hormone deficiencies may also be present. Mutations in the SHH gene have been identified.
- Identifiers
- MONDO:0007819 OMIM:147250Orphanet:2286
- Also known as
- incisors fused · single median maxillary central incisor · single upper central incisor · SMMCI · solitary MEDIAN maxillary central incisor
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