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©The Author(s) 2022.
World J Clin Cases. Aug 26, 2022; 10(24): 8749-8754
Published online Aug 26, 2022. doi: 10.12998/wjcc.v10.i24.8749
Published online Aug 26, 2022. doi: 10.12998/wjcc.v10.i24.8749
Figure 1 Brain magnetic resonance images.
A: T1; B: T2; C: T2 fluid-attenuated inversion recovery; D: Diffusion-weighted imaging.
Figure 2 Whole-exome gene sequencing revealed a compound heterozygous mutation in the VARS2 gene which was derived from the parents.
A-C: VARS2: c.1163(exon11)C>T: Proband (A); Father of the proband (B); Mother of the proband (C); D-F: VARS2: c.1940(exon20)C>T: Proband (D); Father of the proband (E); Mother of the proband (F).
- Citation: Wu XH, Lin SZ, Zhou YQ, Wang WQ, Li JY, Chen QD. VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report. World J Clin Cases 2022; 10(24): 8749-8754
- URL: https://www.wjgnet.com/2307-8960/full/v10/i24/8749.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v10.i24.8749