Publication Name	World Journal of Clinical Cases
Manuscript ID	83518
Country	Romania

Received	2023-01-28 12:13
Peer-Review Started	2023-01-28 12:18
To Make the First Decision
Return for Revision	2023-03-10 09:32
Revised	2023-03-18 21:33
Second Decision	2023-03-27 03:23
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2023-03-27 11:09
Articles in Press	2023-03-27 11:09
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2023-04-07 09:31
Publish the Manuscript Online	2023-04-25 23:32

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/
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Category	Genetics & Heredity
Manuscript Type	Review
Article Title	Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling
Manuscript Source	Invited Manuscript
All Author List	Monica-Cristina Panzaru, Andreea Florea, Lavinia Caba and Eusebiu Vlad Gorduza
ORCID	Author(s) ORCID Number Monica-Cristina Panzaru http://orcid.org/0000-0002-6762-4067 Andreea Florea http://orcid.org/0000-0003-2550-0135 Lavinia Caba http://orcid.org/0000-0001-6327-4461 Eusebiu Vlad Gorduza http://orcid.org/0000-0002-6776-4844
Funding Agency and Grant Number
Corresponding Author	Andreea Florea, MD, Doctor, Department of Medical Genetics - Medical Genetics resident, “Grigore T. Popa” University of Medicine and Pharmacy, 16 University Street , Iasi 700115 , Romania. andreeaflorea97@gmail.com
Key Words	Osteogenesis imperfecta; Heterogeneity; Classification; Molecular mechanism; Genetic counseling; Prophylaxis
Core Tip	Osteogenesis imperfecta (OI) is a genetically heterogeneous systemic collagenous disorder with high phenotypic variability. Recent discoveries of new genes and molecular mechanisms underlying the disease have led to revisions of classical classification. Identifying the causative gene and molecular mechanisms allows a personalized management strategy, accurate family planning, and pregnancy management decisions including options for mode of delivery, or early antenatal OI treatment.
Publish Date	2023-04-25 23:32
Citation	Panzaru MC, Florea A, Caba L, Gorduza EV. Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling. World J Clin Cases 2023; 11(12): 2604-2620
URL	https://www.wjgnet.com/2307-8960/full/v11/i12/2604.htm
DOI	https://dx.doi.org/10.12998/wjcc.v11.i12.2604

Full Article (PDF)	WJCC-11-2604.pdf
Full Article (Word)	WJCC-11-2604.docx
Manuscript File	83518_Auto_Edited-JLW.docx
Answering Reviewers	83518-Answering reviewers.pdf
Audio Core Tip	83518-Audio core tip.mpeg
Conflict-of-Interest Disclosure Form	83518-Conflict-of-interest statement.pdf
Copyright License Agreement	83518-Copyright license agreement.pdf
Non-Native Speakers of English Editing Certificate	83518-Language certificate.pdf
Peer-review Report	83518-Peer-review(s).pdf
Scientific Misconduct Check	83518-Bing-Liu XF-2.png
Scientific Editor Work List	83518-Scientific editor work list.pdf