Literature DB >> 11498754

Successful mismatched sibling cord blood transplant in Hb Bart's disease.

X Zhou1, S Y Ha, G C Chan, C W Luk, V Chan, B Hawkins, Y H Lam, R H Liang, Y L Lau.   

Abstract

A 20-month-old girl with Hb Bart's disease, who had survived neonatal complications, underwent HLA-DR antigen mismatched sibling cord blood transplantation successfully. Immune thrombocytopenia, which occurred around 2.5 months after transplant, responded to intravenous gamma-globulin. The fetal hemoglobin level rose to a peak of 52.3% on day +69 post transplant and declined gradually during the following year. Ten percent of hemoglobin Bart's was detected 2 months after transplant and this reflects the alpha-thalassemia trait of the donor.

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Year:  2001        PMID： 11498754     DOI： 10.1038/sj.bmt.1703104

Source DB:  PubMed          Journal:  Bone Marrow Transplant        ISSN： 0268-3369            Impact factor:   5.483


  10 in total

1.  Normal cognitive functioning in a patient with Hb Bart's hydrops successfully cured by hematopoietic SCT.

Authors:  B Pongtanakul; K Sanpakit; V Chongkolwatana; V Viprakasit
Journal:  Bone Marrow Transplant       Date:  2013-08-26       Impact factor: 5.483

Review 2.  An international registry of survivors with Hb Bart's hydrops fetalis syndrome.

Authors:  Duantida Songdej; Christian Babbs; Douglas R Higgs
Journal:  Blood       Date:  2017-01-05       Impact factor: 22.113

Review 3.  Clinical manifestations of α-thalassemia.

Authors:  Elliott P Vichinsky
Journal:  Cold Spring Harb Perspect Med       Date:  2013-05-01       Impact factor: 6.915

Review 4.  Hydrops fetalis caused by homozygous alpha-thalassemia and Rh antigen alloimmunization: report of a survivor and literature review.

Authors:  Divya-Devi Joshi; H James Nickerson; Michael J McManus
Journal:  Clin Med Res       Date:  2004-11

Review 5.  Advances in the management of α-thalassemia major: reasons to be optimistic.

Authors:  Paulina Horvei; Tippi MacKenzie; Sandhya Kharbanda
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2021-12-10

Review 6.  Alpha-thalassaemia.

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

7.  Fetal gene therapy of alpha-thalassemia in a mouse model.

Authors:  Xiao-Dong Han; Chin Lin; Judy Chang; Michel Sadelain; Y W Kan
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-11       Impact factor: 11.205

8.  Successful matched unrelated donor stem cell transplant in Hemoglobin Bart's disease.

Authors:  M Y Elsaid; C M Capitini; C A Diamond; M Porte; M Otto; K B DeSantes
Journal:  Bone Marrow Transplant       Date:  2016-06-13       Impact factor: 5.483

Review 9.  In utero hematopoietic cell transplantation for hemoglobinopathies.

Authors:  S Christopher Derderian; Cerine Jeanty; Mark C Walters; Elliott Vichinsky; Tippi C MacKenzie
Journal:  Front Pharmacol       Date:  2015-01-12       Impact factor: 5.810

10.  Association of Tissue-Specific DNA Methylation Alterations with α-Thalassemia Southeast Asian Deletion.

Authors:  Tanapat Pangeson; Phanchana Sanguansermsri; Torpong Sanguansermsri; Teerapat Seeratanachot; Narutchala Suwanakhon; Metawee Srikummool; Worasak Kaewkong; Khwanruedee Mahingsa
Journal:  Genet Epigenet       Date:  2017-11-15
  10 in total

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