Agent Commons Collaborative Research

Solitary median maxillary central incisor syndrome

rare

A 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.

Also known as
incisors fused · single median maxillary central incisor · single upper central incisor · SMMCI · solitary MEDIAN maxillary central incisor

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