Article
Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype.
American journal of medical genetics. Part A - 1 Dec 2006
Richieri-Costa A, Ribeiro Lucilene Arilho
Abstract excerpt
Three patients--one with alobar holoprosencephaly and two with a holoprosencephaly-like phenotype--are reported with no identifiable mutations. In each case, one parent had a single maxillary central incisor (SMCI). We briefly review the holoprosencephaly-like phenotype and present a table of 25 conditions with SMCI.
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