An Atypical 0.73 MB Microduplication of 22q11.21 and a Novel Sall4 Missense Mutation Associated with Thumb Agenesis and Radioulnar Synostosis

作者：Diehl Adam; Mu Weiyi; Batista Denise; Gunay Aygun Meral^*

来源：American Journal of Medical Genetics, Part A, 2015, 167(7): 1644-1649.

DOI：10.1002/ajmg.a.37066

• chromosome 22q11.21 microduplication syndrome
• SALL4
• thumb agenesis
• radioulnar synostosis

We describe a 0.73 Mb duplication of chromosome 22q11.21 between LCR-B and LCR-D and a missense mutation in a conserved C2H2 zinc finger domain of SALL4 in a cognitively normal patient with multiple skeletal anomalies including radioulnar synostosis, thumb aplasia, butterfly vertebrae, rib abnormalities, and hypoplasia of the humeral and femoral epiphyses. 22q11.21 is a common site for microdeletions and their reciprocal microduplications as a result of nonallelic homologous recombination between its multiple low copy repeat regions (LCR). DiGeorge /Velocardiofacial syndrome (DG/VCFS) is classically caused by a 3 Mb deletion between LCR-A and LCR-D or a 1.5 Mb deletion between LCR-A and LCR-B. The reciprocal syndrome to DG/VCFS is the recently described 22q11.2 microduplication, which usually presents with the typical 3 Mb or 1.5 Mb duplication. Numerous atypical deletions and duplications have been reported between other LCRs. Typically, SALL4-related Duane-radial ray syndrome is caused by deletions or nonsense mutations; the only missense SALL4 mutation described prior was thought to result in gain of function and produced cranial midline defects. The skeletal anomalies presented in this report have not been previously described in association with 22q11.2 microduplication nor SALL4 mutations.

• 出版日期2015-7
• 单位河北医科大学