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6/30/2023 1:20:05 PM | Browse: 131 | Download: 374
Publication Name World Journal of Clinical Cases
Manuscript ID 82902
Country Saudi Arabia
Received
2022-12-29 09:57
Peer-Review Started
2022-12-29 09:58
To Make the First Decision
Return for Revision
2023-02-17 02:43
Revised
2023-03-19 08:05
Second Decision
2023-04-20 03:10
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2023-04-20 07:19
Articles in Press
2023-04-20 07:19
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2023-06-25 01:45
Publish the Manuscript Online
2023-06-30 12:54
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 Copyright: © The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved.
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Ophthalmology
Manuscript Type Case Report
Article Title Unique Roberts syndrome with bilateral congenital glaucoma: A case report
Manuscript Source Unsolicited Manuscript
All Author List Amar Almulhim, Basamat Almoallem, Ehab Alsirrhy and Essam A Osman
Funding Agency and Grant Number
Corresponding Author Amar Almulhim, MD, Academic Fellow, Department of Ophthalmology, King Saud University, King Abdullah Road, Riyadh 11411, Saudi Arabia. dr.ammar1412@gmail.com
Key Words Roberts syndrome; Roberts-SC phocomelia syndrome; Phocomelia; Congenital glaucoma; Karyotype; Whole exome sequencing; Case report
Core Tip Roberts syndrome (RS) is an extremely rare disease characterized by a combination of deformities in the lower and/or upper extremities in association with other organ abnormalities. We provide here the first reported case of RS associated with bilateral congenital glaucoma. Bilateral non-penetrating glaucoma surgery was performed to control intraocular pressure and the outcome was excellent.
Publish Date 2023-06-30 12:54
Citation Almulhim A, Almoallem B, Alsirrhy E, Osman EA. Unique Roberts syndrome with bilateral congenital glaucoma: A case report. World J Clin Cases 2023; 11(19): 4635-4639
URL https://www.wjgnet.com/2307-8960/full/v11/i19/4635.htm
DOI https://dx.doi.org/10.12998/wjcc.v11.i19.4635
Full Article (PDF) WJCC-11-4635-with-cover.pdf
Full Article (Word) WJCC-11-4635.docx
Manuscript File 82902_Auto_Edited-JLW.docx
Answering Reviewers 82902-Answering reviewers.pdf
Audio Core Tip 82902-Audio core tip.m4a
Conflict-of-Interest Disclosure Form 82902-Conflict-of-interest_statement.pdf
Copyright License Agreement 82902-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s) 82902-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate 82902-Language certificate.pdf
Peer-review Report 82902-Peer-review(s) .pdf
Scientific Misconduct Check 82902-Bing-Liu XF-2.png
Scientific Editor Work List 82902-Scientific editor work list.pdf