| Literature DB >> 8280739 |
L J Lo1, M S Noordhoff, C S Huang, K T Chen, Y R Chen.
Abstract
A patient with bilateral complete cleft of the lip and palate (CLP) had a proximal deletion of the long arm of chromosome 1 (1q). This rare chromosomal abnormality was characterized by pre- and postnatal growth retardation, psychomotor retardation, and specific craniofacial and other systemic anomalies. There is a high incidence of CLP in proximal 1q deletion syndrome, especially bilateral CLP. Twelve other cases reported in the literature having this deletion and associated anomalies were reviewed.Entities:
Mesh:
Year: 1993 PMID: 8280739 DOI: 10.1597/1545-1569_1993_030_0586_pdotla_2.3.co_2
Source DB: PubMed Journal: Cleft Palate Craniofac J ISSN: 1055-6656