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©The Author(s) 2022.
World J Clin Cases. Oct 26, 2022; 10(30): 11031-11036
Published online Oct 26, 2022. doi: 10.12998/wjcc.v10.i30.11031
Published online Oct 26, 2022. doi: 10.12998/wjcc.v10.i30.11031
Table 1 Peripheral blood whole genome microarray analysis the results showed that the patient's chromosome was male karyotype, and there were three chromosomal abnormalities
| Chromosome | Exception type | Chromosome abnormal zones and genome coordinates (ISCN2013) | Abnormal size in kbp | Clinical significance |
| 5 | Loss | arr (hg19) 5p 15.2 pter (113576-13464559) × 1 | 13351 | Abnormal correlation of hereditary diseases |
| 14 | Loss | arr (hg19)14q 11.2 (22510337-22969566) × 1 | 459 | Benign CNV changes |
| 14 | Gain | arr (hg19) 14q 32.33 (106251069-106751178) × 3 | 500 | - |
- 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