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Articles Published Processes
11/25/2020 2:44:04 PM | Browse: 571 | Download: 1269
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Received |
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2020-06-13 05:16 |
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Peer-Review Started |
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2020-06-13 05:16 |
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To Make the First Decision |
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Return for Revision |
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2020-09-13 06:22 |
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Revised |
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2020-09-22 12:00 |
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Second Decision |
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2020-10-14 10:04 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2020-10-20 03:56 |
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Articles in Press |
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2020-10-20 03:56 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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2020-10-25 02:36 |
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Typeset the Manuscript |
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2020-11-18 09:38 |
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Publish the Manuscript Online |
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2020-11-25 14:44 |
| 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: http://creativecommons.org/Licenses/by-nc/4.0/ |
| Copyright |
© The Author(s) 2020. 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 |
Pediatrics |
| Manuscript Type |
Case Report |
| Article Title |
Gene diagnosis of infantile neurofibromatosis type I: A case report
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Meng-Zhu Li, Lin Yuan and Zhi-Qiang Zhuo |
| ORCID |
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| Funding Agency and Grant Number |
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| Corresponding Author |
Zhi-Qiang Zhuo, MD, Chief Doctor, Department of Infectious Diseases, Xiamen Children's Hospital, Children’s Hospital of Fudan University Xiamen Branch, No. 92, Yibin Road, Huli District, Xiamen 361006, Fujian Province, China. q661113@sina.cn |
| Key Words |
Genetic diagnosis; Eurofibromatosis type I; Neurofibromatosis; Infant; Case report; Clinical manifestations |
| Core Tip |
Neurofibromatosis type I (NF1) is a common autosomal dominant disorder with clinical symptoms in the skin, nervous system, skeleton, and eyes. NF1 development is related to gene deletion, and its incidence rate is about 1/3000. It is rare among children, especially infants. This report presents the case of a 3-mo old male infant who was diagnosed with NF1. We believe that our study makes a significant contribution to the literature because this information will be of practical use to clinicians for management of similar conditions and encourage other researchers to validate our findings. |
| Publish Date |
2020-11-25 14:44 |
| Citation |
Li MZ, Yuan L, Zhuo ZQ. Gene diagnosis of infantile neurofibromatosis type I: A case report. World J Clin Cases 2020; 8(22): 5678-5683 |
| URL |
https://www.wjgnet.com/2307-8960/full/v8/i22/5678.htm |
| DOI |
https://dx.doi.org/10.12998/wjcc.v8.i22.5678 |
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