SEARCH

SEARCH BY CITATION

Keywords:

  • hypotelorism;
  • midface deficiency;
  • cleft lip/palate;
  • absent mutations

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.