Publication Name	World Journal of Clinical Pediatrics
Manuscript ID	110750
Country	Jordan

Received	2025-06-17 01:20
Peer-Review Started	2025-06-17 01:20
To Make the First Decision
Return for Revision	2025-06-23 01:48
Revised	2025-06-23 16:33
Second Decision	2025-08-01 02:40
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2025-08-01 12:01
Articles in Press	2025-08-01 12:01
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2025-09-01 05:58
Publish the Manuscript Online	2025-10-31 15:02

ISSN	2219-2808 (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	Pediatrics
Manuscript Type	Case Report
Article Title	Exploring Roberts syndrome, unique manifestations in a four-month-old infant and genetic findings: A case report
Manuscript Source	Invited Manuscript
All Author List	Samia Aziz Sulaiman, Laith Kaylani, Qusai Manaseer and Dina K Mohammed
ORCID	Author(s) ORCID Number Samia Aziz Sulaiman http://orcid.org/0009-0001-2937-9064
Funding Agency and Grant Number
Corresponding Author	Samia Aziz Sulaiman, MD, School of Medicine, The University of Jordan, Queen Rania Street, Amman 11942, Jordan. samia.sulaiman2003@gmail.com
Key Words	Growth disorders; Metabolic; Mutations; Case report
Core Tip	Roberts syndrome is a rare but severe autosomal recessive disorder caused by mutations in the ESCO2 gene, characterized by limb malformations, growth restriction, and multisystem involvement. This case highlights the urgent need for early detection through integrated prenatal imaging and genetic testing, especially in consanguineous families, to enable timely diagnosis, guide clinical management, and support informed reproductive decision-making.
Publish Date	2025-10-31 15:02
Citation	<p>Sulaiman SA, Kaylani L, Manaseer Q, Mohammed DK. Exploring Roberts syndrome, unique manifestations in a four-month-old infant and genetic findings: A case report. <i>World J Clin Pediatr</i> 2025; 14(4): 110750</p>
URL	https://www.wjgnet.com/2219-2808/full/v14/i4/110750.htm
DOI	https://dx.doi.org/10.5409/wjcp.v14.i4.110750

Full Article (PDF)	WJCP-14-110750-with-cover.pdf
CARE Checklist–2016	110750-CARE-Checklist-2016.pdf
Manuscript File	110750_Auto_Edited_015704.docx
Answering Reviewers	110750-answering-reviewers.pdf
Audio Core Tip	110750-audio.mp3
Conflict-of-Interest Disclosure Form	110750-conflict-of-interest-statement.pdf
Copyright License Agreement	110750-copyright-assignment.pdf
Signed Consent for Treatment Form(s) or Document(s)	110750-informed-consent-statement.pdf
Non-Native Speakers of English Editing Certificate	110750-non-native-speakers.pdf
Peer-review Report	110750-peer-reviews.pdf
Scientific Misconduct Check	110750-scientific-misconduct-check.png
Scientific Editor Work List	110750-scientific-editor-work-list.pdf
CrossCheck Report	110750-crosscheck-report.pdf