Neonatal Cri du chat syndrome with atypical facial appearance: A case report

doi:10.12998/wjcc.v10.i30.11031

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Oct 26, 2022 (publication date) through Dec 28, 2024

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Oct 26, 2022; 10(30): 11031-11036
Published online Oct 26, 2022. doi: 10.12998/wjcc.v10.i30.11031

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Figure 2 Analysis of 24 human chromosomes by whole genome microarray in peripheral blood. Autosomes 1-22 and sex chromosomes X and Y were detected. The results of chromosomal abnormalities showed deletion of chromosome 5 (orange), amplification of chromosome 5 (blue)，and heterozygous deletion of chromosome 23 (purple).

Citation: Bai MM, Li W, Meng L, Sang YF, Cui YJ, Feng HY, Zong ZT, Zhang HB. Neonatal Cri du chat syndrome with atypical facial appearance: A case report. World J Clin Cases 2022; 10(30): 11031-11036
URL: https://www.wjgnet.com/2307-8960/full/v10/i30/11031.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i30.11031