Literature DB >> 16339648

Alpha-thalassemia: Hb H disease and Hb Barts hydrops fetalis.

David H K Chui1.   

Abstract

alpha-Thalassemia mutations are one of the most common mutations of man, and they cause Hb H disease and Hb Barts hydrops fetalis. Hb H disease is not necessarily a benign disorder as has been generally thought. Furthermore, in southern China and in Southeast Asia, there are 2-3 times more fetuses afflicted with the invariably fatal Hb Barts hydrops fetalis than with the beta-thalassemia major or intermedia. These findings underscore the public health importance of these hereditary disorders, and they call for better education, diagnosis, treatment, prevention, and research for these diseases.

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Year:  2005        PMID: 16339648     DOI: 10.1196/annals.1345.004

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  23 in total

1.  Hemoglobin H disease in Muscat, Oman - A 5 year study.

Authors:  Suresh Venugopal; Suchata Dhuri; Khalid Bait Al Jabal; Alphonsa Shaju
Journal:  Oman Med J       Date:  2008-04

2.  The Adverse Effects of Pregnancies Complicated by Hemoglobin H (HBH) Disease.

Authors:  Maryam Rabiee; Jalal-Aldin Shams; Nafiseh Zafargandie
Journal:  Iran J Pathol       Date:  2015

3.  Screening and counseling for thalassemia.

Authors:  David H K Chui; Melody J Cunningham; Hong-Yuan Luo; Lawrence C Wolfe; Ellis J Neufeld; Martin H Steinberg
Journal:  Blood       Date:  2006-02-15       Impact factor: 22.113

4.  Molecular characterization of Hb H disease in southern Thailand.

Authors:  Kesara Nittayaboon; Chamnong Nopparatana
Journal:  Int J Hematol       Date:  2018-07-13       Impact factor: 2.490

Review 5.  Diagnosis and management of heart failure in the fetus.

Authors:  B Davey; A Szwast; J Rychik
Journal:  Minerva Pediatr       Date:  2012-10       Impact factor: 1.312

Review 6.  Alpha-thalassaemia.

Authors:  Cornelis L Harteveld; Douglas R Higgs
Journal:  Orphanet J Rare Dis       Date:  2010-05-28       Impact factor: 4.123

Review 7.  The prevention of thalassemia.

Authors:  Antonio Cao; Yuet Wai Kan
Journal:  Cold Spring Harb Perspect Med       Date:  2013-02-01       Impact factor: 6.915

8.  Prenatal diagnosis of α- and β-thalassemias in southern Thailand.

Authors:  Chamnong Nopparatana; Chawadee Nopparatana; Vannarat Saechan; Sataron Karnchanaopas; Korntip Srewaradachpisal
Journal:  Int J Hematol       Date:  2019-10-28       Impact factor: 2.490

9.  Reliable detection of paternal SNPs within deletion breakpoints for non-invasive prenatal exclusion of homozygous α-thalassemia in maternal plasma.

Authors:  Ti-Zhen Yan; Qiu-Hua Mo; Ren Cai; Xue Chen; Cui-Mei Zhang; Yan-Hui Liu; Ya-Jun Chen; Wan-Jun Zhou; Fu Xiong; Xiang-Min Xu
Journal:  PLoS One       Date:  2011-09-29       Impact factor: 3.240

10.  PTD-mediated delivery of α-globin chain into Κ-562 erythroleukemia cells and α-thalassemic (HBH) patients' RBCs ex vivo in the frame of Protein Replacement Therapy.

Authors:  Androulla N Miliotou; Dionysia Papagiannopoulou; Efthymia Vlachaki; Martina Samiotaki; Dimitra Laspa; Stamatia Theodoridou; Asterios S Tsiftsoglou; Lefkothea C Papadopoulou
Journal:  J Biol Res (Thessalon)       Date:  2021-07-20       Impact factor: 1.889

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