<?xml version="1.0" encoding="utf-8"?>
			<journal>
			<title>Journal of Pediatric Perspectives</title>
			<title_fa></title_fa>
			<short_title>JPP; J Ped Perspect</short_title>
			<subject>Medical Sciences</subject>
			<web_url>https://jpp.mums.ac.ir/</web_url>
			<journal_hbi_system_id>0</journal_hbi_system_id>
			<journal_hbi_system_user></journal_hbi_system_user>
			<journal_id_issn></journal_id_issn>
			<journal_id_issn_online>3060-7205</journal_id_issn_online>
			<journal_id_pii></journal_id_pii>
			<journal_id_doi></journal_id_doi>
			<journal_id_iranmedex></journal_id_iranmedex>
			<journal_id_magiran></journal_id_magiran>
			<journal_id_sid></journal_id_sid>
			<journal_id_nlai></journal_id_nlai>
			<journal_id_science></journal_id_science>
			<language>en</language>
			<pubdate>
				<type>jalali</type>
				<year>0</year>
				<month>0</month>
				<day>1</day>
			</pubdate>
			<pubdate>
				<type>gregorian</type>
				<year>2014</year>
				<month>5</month>
				<day>1</day>
			</pubdate>
			<volume>2</volume>
			<number>2.3</number>
			<publish_type>online</publish_type>
			<publish_edition>1</publish_edition>
			<article_type>fulltext</article_type>
			<articleset><article>
				<language>en</language>
				<article_id_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Bone Marrow Transplant (BMT) is the Main Cureavailable for Thalassamia</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa></content_type_fa>
				<content_type></content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Introduction:
The thalassamias refer to a diverse group of hemoglobin disorders characterized by a reduced synthesis of  one or more of globin chains (α,β, γ, δβ,γδβ, δ and εγδβ).The main cure available today for thalassamia is bone marrow transplantation (BMT)  from compatible donor.On December 3, 1981 a 14-month-old child with β-thalassemia major recieved BMT from his HLA-identical sister in Seattle.On December 17, 1981 the Pesaro team performed a transplant in a 16-year old thalassamia, using marrow from his HLA-identical brother.This patient rejected the graft.
Methods:
In our study, twenty twotransfusion dependentthalassemia patients were recruited.When HLA matched donor was detected, he or she was checked for asymptomatic infection, electerolytes and endocrinopathy. Donors were either heterozygous for β-thalassemia or normal homozygous.
Results:
In our center 22 transfusion dependent hemglobinopathies (10 girls and 12 boys,age3-26y, Mean=15.6y) underwent to HSCT from September 2010 until May  2014.Graft failure happened in 3 patients. Retransplantation was done for one patient who was X variant hemoglobinopathy.Twenty patients were disease free and didn`t need to transfusion after BMT. Although in our BMT center , few thalassemia patients underwent to transplantation, 20 of 22 were independent to blood transfusion after transplantation. One patient who underwent to retransplantation is undependent to transfusion.
Conclusion:
Patients and their family were very pleasured and satisfied. We suggest all patients with β-thalassemia who have HLA-identical related donors should be transplanted as soon as possible.
 
 
Keyword: Bone Marrow Transplant, HLA-identical, β-thalassemia.
 ]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Oral Presentation</keyword>
				<start_page>24</start_page>
				<end_page>24</end_page>
				<web_url>https://jpp.mums.ac.ir/article_2673.html</web_url>
			<author_list><author>
				<first_name>Hassan</first_name>
				<middle_name></middle_name>
				<last_name>Mahmoodi Nesheli</last_name>
				<suffix></suffix>
				<first_name_fa></first_name_fa>
				<middle_name_fa></middle_name_fa>
				<last_name_fa></last_name_fa>
				<suffix_fa></suffix_fa>
				<email></email>
				<code>9672</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Pediatric Hematologist Oncologist and BMT Flowship Non-Communicable Pediatrics Diseases Research Center, Babol University of Medical Sciences, Babol, Iran.</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article>
			</articleset>
			</journal>