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Chromosome 22q11.21 and 11p15.4 microdeletions confirmed by DNA high throughput sequencing analysis in one patient with asymmetric cry syndrome：Case report and review of the literature
  • +3
  • Yonghong Pang,
  • Yang Yu,
  • Xiaoyi Deng,
  • Qian Liu,
  • Junmei Yan,
  • Xiangyu Gao
Yonghong Pang
center for medical neonatal Xuzhou maternity and child health hospital

Corresponding Author:[email protected]

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Yang Yu
Center for Medical Neonatal, Xuzhou Maternity and Child Health Hospital
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Xiaoyi Deng
Center for Medical Neonatal, Xuzhou Maternity and Child Health Hospital
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Qian Liu
Center for Medical Neonatal, Xuzhou Maternity and Child Health Hospital
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Junmei Yan
Center for Medical Neonatal, Xuzhou Maternity and Child Health Hospital
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Xiangyu Gao
Xuzhou Affiliated Hospital of East South University Xuzhou, Jiangsu, China
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Abstract

The case report describes a newborn case of ACS based on clinical presentation(s) and microdeletions of 22q11.21 and 11p15.4 using DNA high throughput sequencing analysis. This finding has implications for ACS diagnosis and overcomes the limitations associated with FISH by using the DNA high throughput sequencing across the whole genome.

Peer review status:ACCEPTED

11 Oct 2020Submitted to Clinical Case Reports
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17 Oct 2020Submission Checks Completed
17 Oct 2020Assigned to Editor
30 Oct 2020Reviewer(s) Assigned
05 Jan 2021Review(s) Completed, Editorial Evaluation Pending
06 Jan 2021Editorial Decision: Revise Minor
24 Feb 20211st Revision Received
26 Feb 2021Submission Checks Completed
26 Feb 2021Assigned to Editor
26 Feb 2021Review(s) Completed, Editorial Evaluation Pending
01 Mar 2021Editorial Decision: Accept