Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype

Authors

  • A. Richieri-Costa,

    Corresponding author
    1. Serviço de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, São Paulo, Brazil
    • HRAC-USP, PO Box 620, Rua Silvio Marchione 320, CEP 17012-900, Bauru, SP, Brasil.
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  • Lucilene Arilho Ribeiro

    1. Serviço de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, São Paulo, Brazil
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  • How to cite this article: Richieri-Costa A, Ribeiro LA. 2006. Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype. Am J Med Genet Part A 140A:2594–2597.

Abstract

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. © 2006 Wiley-Liss, Inc.

Ancillary