A de novo triplication on 2q22.3 including the entire ZEB2 gene associated with global developmental delay, multiple congenital anomalies and behavioral abnormalities

作者：Yuan, Haiming; Zhang, Lina; Chen, Mengfan; Zhu, Junping; Meng, Zhe; Liang, Liyang^*

来源：Molecular Cytogenetics, 2015, 8(1): 99.

DOI：10.1186/s13039-015-0206-8

• Mowat-Wilson syndrome
• Distinctive facial features
• Intellectual disability
• Developmental delay
• Congenital anomalies
• Behavioral abnormalities
• ZEB2-triplication

Background: Mowat-Wilson syndrome (MWS) is a genetic condition characterized by distinctive facial features, moderate to severe intellectual disability, developmental delay and multiple congenital anomalies. MWS is caused by heterozygous mutations or deletions of the ZEB2 gene located on chromosome 2q22.3. At present, over 190 cases with mutations and deletions involving the ZEB2 gene have been reported, but triplication or duplication of reciprocal region of Mowat-Wilson syndrome has never been reported.
Case Presentation: Here we report a 2-year-2-month-old boy carrying a de novo 2.9 Mb complex copy number gain at 2q22.3 involving triplication of ZEB2 gene. The boy is characterized by intrauterine growth retardation, hypotonia, cognitive impairment, multiple congenital anomalies and behavioral abnormalities.
Conclusion: This case provides evidence that triplication of ZEB2 gene may be clinical significance and ZEB2 gene is likely to be a dosage sensitive gene.

• 出版日期2015-12-23
• 单位广州医科大学; 中山大学