Publication Name	World Journal of Clinical Cases
Manuscript ID	34012
Country	Brazil

Received	2017-03-21 09:09
Peer-Review Started	2017-03-23 17:56
To Make the First Decision	2017-06-15 06:25
Return for Revision	2017-06-15 06:49
Revised	2017-06-23 14:27
Second Decision	2017-07-26 06:25
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2017-08-02 20:27
Articles in Press	2017-08-02 20:27
Publication Fee Transferred	2017-08-09 19:01
Edit the Manuscript by Language Editor
Typeset the Manuscript	2017-10-11 08:28
Publish the Manuscript Online	2017-10-13 09:39

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/
Copyright	© The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved.
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Website	http://www.wjgnet.com

Category	Medicine, Research & Experimental
Manuscript Type	Case Report
Article Title	Juvenile hemochromatosis: HAMP mutation and severe iron overload treated with phlebotomies and deferasirox
Manuscript Source	Unsolicited Manuscript
All Author List	Manuel A Lescano, Letícia C Tavares and Paulo C J L Santos
ORCID	Author(s) ORCID Number Manuel A Lescano http://orcid.org/0000-0002-5154-5372 Letícia C Tavares http://orcid.org/0000-0001-7278-0999 Paulo C J L Santos http://orcid.org/Santos
Funding Agency and Grant Number
Corresponding Author	Paulo C J L Santos, PhD, Adjunct Professor, Laboratory of Genetics and Molecular Cardiology, Heart Institute (InCor), University of Sao Paulo Medical School, 03 de Maio, St. INFAR, 4th floor, Vila Clementino, SP 04044-020, São Paulo, Brazil. pacaleb@usp.br
Key Words	Genetic disease; Juvenile hemochromatosis; HAMP gene; Mutation; Iron chelation
Core Tip	A 29-year-old Brazilian woman, from a city in the countryside of the State of Bahia, Brazil, was referred to our service in 2015 because of a hepatomegaly clinical condition, detected by imaging exam. This case study reports a patient with juvenile hemochromatosis condition due to HAMP mutation (g.47G>A) treated with phlebotomies and deferasirox, which were able to normalize iron levels and improve symptoms.
Publish Date	2017-10-13 09:39
Citation	Lescano MA, Tavares LC, Santos PCJL. Juvenile hemochromatosis: HAMP mutation and severe iron overload treated with phlebotomies and deferasirox. World J Clin Cases 2017; 5(10): 381-383
URL	http://www.wjgnet.com/2307-8960/full/v5/i10/381.htm
DOI	http://dx.doi.org/10.12998/wjcc.v5.i10.381

Full Article (PDF)	WJCC-5-381.pdf
Full Article (Word)	WJCC-5-381.doc
Manuscript File	34012-Review.docx
Answering Reviewers	34012-Answering reviewers.pdf
Audio Core Tip	34012-Audio core tip.wav
Conflict-of-Interest Disclosure Form	34012-Conflict-of-interest statement.pdf
Copyright License Agreement	34012-Copyright assignment.pdf
Signed Informed Consent Form(s) or Document(s)	34012-Informed consent statement.pdf
Institutional Review Board Approval Form or Document	34012-Institutional review board statement.pdf
Non-Native Speakers of English Editing Certificate	34012-Language certificate.pdf
Peer-review Report	34012-Peer-review(s).pdf
Scientific Misconduct Check	34012-Scientific misconduct check.pdf
Scientific Editor Work List	34012-Scientific editor work list.pdf