Publication Name	World Journal of Clinical Cases
Manuscript ID	49852
Country	China

Received	2019-06-25 05:53
Peer-Review Started	2019-06-27 13:17
To Make the First Decision	2019-08-02 03:24
Return for Revision	2019-08-26 08:58
Revised	2019-08-29 09:18
Second Decision	2019-09-06 10:01
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2019-09-11 06:05
Articles in Press	2019-09-11 06:05
Publication Fee Transferred
Edit the Manuscript by Language Editor	2019-10-14 07:35
Typeset the Manuscript	2019-10-23 06:36
Publish the Manuscript Online	2019-10-26 03:14

ISSN	2307-8960 (online)
Open Access	This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (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	Medicine, Research & Experimental
Manuscript Type	Case Report
Article Title	Recognizable type of pituitary, heart, kidney and skeletal dysplasia mostly caused by SEMA3A mutation: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Fang Hu and Liao Sun
ORCID	Author(s) ORCID Number Fang Hu http://orcid.org/0000-0002-6610-6495 Liao Sun http://orcid.org/0000-0002-1798-0944
Funding Agency and Grant Number
Corresponding Author	Liao Sun, PhD, Chief Doctor, Department of Endocrinology and Metabolism, Fifth Affiliated Hospital Sun Yat-Sen University, Sun Yat-Sen University, Meihuadong Road 52, Zhuhai 519000, Guangdong Province, China. sunliao@mail.sysu.edu.cn
Key Words	Pituitary dysplasia; Heart dysplasia; Kidney dysplasia; Short stature; Cryptorchidism; SEMA3A
Core Tip	The SEMA3A gene is involved in hypothalamic neuron migration, heart development, kidney development, and skeleton metabolism. Mutation of the SEMA3A gene was associated with short stature, low gonadotropin, hypogonadism, thoracic deformity, a high scapula, rib and lower limb deformity, facial deformity (long face, epicanthic folds, backwards ears), and arterial malformation in cases reported before. Here, we report a patient who exhibited pituitary, heart, kidney and skeletal dysplasia caused by new mutation of the SEMA3A gene (c.950A>G).
Publish Date	2019-10-26 03:14
Citation	Hu F, Sun L. Recognizable type of pituitary, heart, kidney and skeletal dysplasia mostly caused by SEMA3A mutation: A case report. World J Clin Cases 2019; In press
URL	https://www.wjgnet.com/2307-8960/full/v7/i20/3310.htm
DOI	https://dx.doi.org/10.12998/wjcc.v7.i20.3310

Full Article (PDF)	WJCC-7-3310.pdf
Full Article (Word)	WJCC-7-3310.docx
Manuscript File	49852-Review-Edited.doc
Answering Reviewers	49852-Answering reviewers.pdf
Audio Core Tip	49852-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	49852-Conflict-of-interest statement.pdf
Copyright License Agreement	49852-Copyright license agreement.pdf
Signed Informed Consent Form(s) or Document(s)	49852-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	49852-Language certificate.pdf
Peer-review Report	49852-Peer-review(s).pdf
Scientific Misconduct Check	49852-Scientific misconduct check.pdf
Scientific Editor Work List	49852-Scientific editor work list.pdf