Publication Name	World Journal of Clinical Cases
Manuscript ID	57504
Country	China

Received	2020-06-13 05:16
Peer-Review Started	2020-06-13 05:16
To Make the First Decision
Return for Revision	2020-09-13 06:22
Revised	2020-09-22 12:00
Second Decision	2020-10-14 10:04
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2020-10-20 03:56
Articles in Press	2020-10-20 03:56
Publication Fee Transferred
Edit the Manuscript by Language Editor	2020-10-25 02:36
Typeset the Manuscript	2020-11-18 09:38
Publish the Manuscript Online	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/
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Category	Pediatrics
Manuscript Type	Case Report
Article Title	Gene diagnosis of infantile neurofibromatosis type I: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Meng-Zhu Li, Lin Yuan and Zhi-Qiang Zhuo
ORCID	Author(s) ORCID Number Meng-Zhu Li http://orcid.org/0000-0002-4522-4345 Lin Yuan http://orcid.org/0000-0002-8417-8388 Zhi-Qiang Zhuo http://orcid.org/0000-0001-6591-2762
Funding Agency and Grant Number
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

Full Article (PDF)	WJCC-8-5678.pdf
Full Article (Word)	WJCC-8-5678.docx
CARE Checklist–2016	57504-CARE-Checklist–2016-revision.pdf
Manuscript File	57504-Review-Filipodia.docx
Answering Reviewers	57504-Answering reviewers.pdf
Audio Core Tip	57504-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	57504-Conflict-of-interest statement.pdf
Copyright License Agreement	57504-Copyright license agreement.pdf
Signed Informed Consent Form(s) or Document(s)	57504-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	57504-Language certificate.pdf
Peer-review Report	57504-Peer-review(s).pdf
Scientific Misconduct Check	57504-Bing-Wang JL-1.jpg
Scientific Misconduct Check	57504-Scientific misconduct check.pdf
Scientific Editor Work List	57504-Scientific editor work list.pdf