Copyright
©The Author(s) 2022.
World J Clin Cases. May 26, 2022; 10(15): 5018-5024
Published online May 26, 2022. doi: 10.12998/wjcc.v10.i15.5018
Published online May 26, 2022. doi: 10.12998/wjcc.v10.i15.5018
Figure 1 A synonymous spontaneous heterozygous mutations found in the LMNA gene in the patient.
Figure 2 No anomalies were found in the LMNA gene in the child’s father as revealed by whole-exome sequencing.
Figure 3 No anomalies were found in the LMNA gene in the child’s mother as revealed by whole-exome sequencing.
- Citation: Zhang SL, Lin SZ, Zhou YQ, Wang WQ, Li JY, Wang C, Pang QM. Clinical manifestations and gene analysis of Hutchinson-Gilford progeria syndrome: A case report. World J Clin Cases 2022; 10(15): 5018-5024
- URL: https://www.wjgnet.com/2307-8960/full/v10/i15/5018.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v10.i15.5018