Publication Name	World Journal of Medical Genetics
Manuscript ID	81957
Country	Australia

Received	2022-11-30 04:05
Peer-Review Started	2022-11-30 04:06
To Make the First Decision
Return for Revision	2023-01-12 04:15
Revised	2023-01-16 00:17
Second Decision	2023-03-01 03:06
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2023-03-01 08:30
Articles in Press	2023-03-01 08:30
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2023-03-09 01:46
Publish the Manuscript Online	2023-03-10 01:48

ISSN	2220-3184 (online)
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Category	Genetics & Heredity
Manuscript Type	Case Report
Article Title	Phenotypic and cytogenetic features of an Iranian child with tetrasomy 18p syndrome: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Sara Esmaeili and Cory J Xian
ORCID	Author(s) ORCID Number Cory J Xian http://orcid.org/0000-0002-8467-2845
Funding Agency and Grant Number
Corresponding Author	Cory J Xian, PhD, Professor, UniSA Clinical and Health Sciences, University of South Australia, North Terrace, GPO Box 2471, Adelaide 5001, SA, Australia. cory.xian@unisa.edu.au
Key Words	Tetrasomy 18p; Phenotypic features; Clinical features; Chromosome abnormality; Cytogenetic analysis; Case report
Core Tip	Gathering data from different cases for the rare tetrasomy 18p chromosome abnormality disorder will facilitate mastering its genotype-phenotype relationship and diagnosis. This report described features for the first time for an Iranian patient. Compared to previously reported cases, this Iranian child displays a uniquely strong sense of smell, some less reported dysmorphic features and ten features generally reported. Her cytogenetic analyses revealed a small marker chromosome with a gain of 14Mb at the 18p arm. Apart from the usual clinical assessments, the non-invasive prenatal genetic testing is suggested to be used as a more accurate screening for detecting tetrasomy 18p.
Publish Date	2023-03-10 01:48
Citation	Esmaeili S, Xian CJ. Phenotypic and cytogenetic features of an Iranian child with tetrasomy 18p syndrome: A case report. World J Med Genet 2023; 11(1): 1-7
URL	https://www.wjgnet.com/2220-3184/full/v11/i1/1.htm
DOI	https://dx.doi.org/10.5496/wjmg.v11.i1.1

Full Article (PDF)	WJMG-11-1.pdf
Full Article (Word)	WJMG-11-1.docx
CARE Checklist–2016	81957-CARE-Checklist–2016-revision.pdf
Manuscript File	81957_Auto_Edited-JLW.docx
Answering Reviewers	81957-Answering reviewers.pdf
Audio Core Tip	81957-Audio core tip.mp3
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Peer-review Report	81957-Peer-review(s).pdf
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Scientific Editor Work List	81957-Scientific editor work list.pdf
CrossCheck Report	81957-CrossCheck report.pdf