| Literature DB >> 15103725 |
Livia Garavelli1, C Zanacca1, G Caselli1, G Banchini1, C Dubourg2, V David2, S Odent2, F Gurrieri3, G Neri3.
Abstract
Solitary median maxillary central incisor (SMMCI) is a rare dental anomaly. It is usually considered as a minor manifestation of holoprosencephaly (HPE). Some reported families had severe cases of HPE in some members and SMMCI in others. Mutations of Sonic Hedgehog (SHH) have been documented in these families. SMMCI has also been found as an isolated finding or together with other anomalies such as microcephaly, short stature, endocrine pathology, and choanal atresia. We describe a patient with SMMCI and a novel SHH mutation: Val332Ala. Copyright 2003 Wiley-Liss, Inc.Entities:
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Year: 2004 PMID: 15103725 DOI: 10.1002/ajmg.a.20685
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802