Pliskin M E, Haber B, Kornbrot A, Madani F, Lally E T
Department of Oral Medicine, University of Pennsylvania School of Dental Medicine, Philadelphia.
Oral Surg Oral Med Oral Pathol. 1988 Oct;66(4):475-9. doi: 10.1016/0030-4220(88)90272-1.
The Greig cephalopolysyndactyly syndrome is an uncommon dysmorphic syndrome characterized by preaxial and postaxial polysyndactyly and minor craniofacial anomalies. It has an autosomal dominant inheritance. A review of the literature has failed to show documentation of any dental or oral abnormalities. Therefore, we report on a patient with Greig syndrome who had a maxillary fibro-osseous lesion and multiple dental and oral abnormalities.
Greig头多指（趾）综合征是一种罕见的畸形综合征，其特征为轴前和轴后多指（趾）畸形以及轻微的颅面异常。它具有常染色体显性遗传。文献综述未能显示有任何牙齿或口腔异常的记录。因此，我们报告了一名患有Greig综合征的患者，该患者有上颌骨纤维性骨病变以及多种牙齿和口腔异常。
