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.
Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype†
Article first published online: 25 SEP 2006
Copyright © 2006 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Special Issue: Thirteenth Annual Robert J. Gorlin Conference on Dysmorphology; Facial and Oral Structures: Molecular Perspectives
Volume 140A, Issue 23, pages 2594–2597, 1 December 2006
How to Cite
Richieri-Costa, A. and Ribeiro, L. A. (2006), Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype. Am. J. Med. Genet., 140A: 2594–2597. doi: 10.1002/ajmg.a.31379
- Issue published online: 21 NOV 2006
- Article first published online: 25 SEP 2006
- Manuscript Accepted: 20 MAY 2006
- Manuscript Received: 4 MAY 2006
- CNPq. Grant Number: 309030/2003-0
- Fogarty award. Grant Number: TW–2–27052-00
- midface deficiency;
- cleft lip/palate;
- absent mutations
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.