Solitary median maxillary central incisor syndrome

MONDO:0007819

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: SMMCI, single median maxillary central incisor, single upper central incisor, solitary median maxillary central incisor syndrome, Fused incisors, SMMCI syndrome, incisors fused, incisors, Fused

0 clinical trials for this condition and its sub-types, 0 tagged with Solitary median maxillary central incisor syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Holoprosencephaly 3 (0) ↑ Microform holoprosencephaly (0)

Including sub-types (0) Tagged with Solitary median maxillary central incisor syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.