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Articles Published Processes
10/21/2022 2:24:59 AM | Browse: 293 | Download: 697
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Received |
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2022-04-24 11:24 |
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Peer-Review Started |
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2022-04-24 11:27 |
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To Make the First Decision |
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Return for Revision |
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2022-06-08 08:42 |
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Revised |
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2022-07-04 12:44 |
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Second Decision |
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2022-09-23 03:26 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2022-09-23 08:25 |
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Articles in Press |
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2022-09-23 08:25 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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2022-09-07 00:00 |
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Typeset the Manuscript |
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2022-09-26 03:03 |
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Publish the Manuscript Online |
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2022-10-21 02:24 |
ISSN |
2307-8960 (online) |
Open Access |
This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
Copyright |
©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. |
Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
Website |
http://www.wjgnet.com |
Category |
Clinical Neurology |
Manuscript Type |
Case Report |
Article Title |
Neonatal Cri du chat syndrome with atypical facial appearance: A case report
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Manuscript Source |
Unsolicited Manuscript |
All Author List |
Meng-Meng Bai, Wen Li, Lin Meng, Yan-Feng Sang, Yu-Jie Cui, Hui-Ying Feng, Zhi-Tao Zong and Hong-Bo Zhang |
ORCID |
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Funding Agency and Grant Number |
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Corresponding Author |
Wen Li, MD, PhD, Professor, Department of Pediatrics, Chengde Central Hospital, Chengde Medical University, No. 66 Guangren Avenue, Shuangqiao District, Chengde 067000, Hebei Province, China. wenwen9155@sina.com |
Key Words |
CdCS; Gene; Chromosome karyotype; Neonatal; Case report |
Core Tip |
A 2-d-old male child presented to our hospital with poor postnatal reaction and poor milk intake. The baby's crying and sucking is weak, reaction and feeding time is poor and the baby has nausea and vomiting. Karyotype analysis showed that the chromosomes were 46, XY, deletion (5) p15. Whole genome microarray analysis (named ISCN2013) showed that the chromosomes of the child were male karyotypes and contained three chromosomal abnormalities. Among them, loss of 5p15.2pter (113576-13464559) was associated with cat call syndrome. After a 3 mo of follow-up, the child still vomited repeatedly, had poor milk intake, did not return to normal growth, had developmental retardation and had a poor directional response. |
Publish Date |
2022-10-21 02:24 |
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 |
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