Department of Otolaryngology, University of Michigan, Ann Arbor, USA.
Am J Med Genet A. 2011 Mar;155A(3):612-7. doi: 10.1002/ajmg.a.33808. Epub 2011 Feb 22.
We describe a patient with multiple congenital anomalies including tracheobronchomalacia, CT-proven metopic craniosynostosis, glandular hypospadias and severe ventral chordee, torticollis, esotropia, strabismus, fifth finger clinodactyly, hallux valgus, and global developmental delay. Using high resolution chromosomal microarray analysis, we identified a de novo deletion of 555 kb on chromosome 16p13.3, 444 kb telomeric to the CREBBP gene and 623 kb centromeric of PKD1. Review of the literature revealed numerous reports of individuals with deletions involving adjacent regions including CREBBP, but only one overlapping with this isolated region of 16p13.3. Haploinsufficiency for one or more of the 25 candidate genes in the deleted genomic region may be responsible for these clinical features. No copy number variants (CNVs) span the entire region, but several small CNVs within the 555 kb genomic region reduce the likelihood for effects due to haploinsufficiency to 18 genes.
我们描述了一位患有多种先天性异常的患者,包括气管支气管软化症、CT 证实的额缝早闭、性腺发育不全性尿道下裂和严重的腹侧索状弯曲、斜颈、内斜视、斜视、第五指弯指畸形、拇外翻和全面发育迟缓。使用高分辨率染色体微阵列分析,我们在 16p13.3 染色体上发现了一个 555 kb 的缺失,该缺失位于 CREBBP 基因的 444 kb 端粒和 PKD1 的 623 kb 着丝粒处。文献复习显示,许多涉及相邻区域的 CREBBP 缺失的个体报告,而仅一个与 16p13.3 的孤立区域重叠。缺失基因组区域中 25 个候选基因之一或多个的单倍不足可能是这些临床特征的原因。没有跨越整个区域的拷贝数变异 (CNVs),但 555 kb 基因组区域内的几个小的 CNVs 将由于单倍不足而导致的效应的可能性降低到 18 个基因。