Hb Fairfax [HBB:c.285_286insGAGCTGCACTGTGAC] in a Brazilian patient with severe hemolytic anemia—identification and functional study-Reference-Cited by-同舟云学术

Hb Fairfax [HBB:c.285_286insGAGCTGCACTGTGAC] in a Brazilian patient with severe hemolytic anemia—identification and functional study

Published:2019-06-28 Issue:9 Volume:98 Page:2253-2255
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Jorge S. E.,Lanaro C.,Albuquerque D. M.,Nascimento P. H.,Pedroso G. A.,Oliveira S. C.,Grigoleto M. R. P.,Santos M. N. N.,Costa F. F.,Sonati M. F.^ORCID

Funder

National Council for Scientific and Technological Development - CNPq/Brazil

São Paulo Research Foundation

Coordination for the Improvement of Higher Education Personnel (CAPES)/Brazil

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00277-019-03728-5.pdf

Reference9 articles.

1. Greenberg J, Fairbanks VF, Hoyer J, Thibodeau SN, Fairfax VA (1997) Hemoglobin Fairfax, a tandem duplication of β90–94 inserted between β94–β95 (proved by DNA sequence analysis): a previously undescribed unstable hemoglobin variant associated with severe hemolytic anemia and stroke during early childhood [abstract]. Blood 90(Suppl. 1):27B

2. Akbari TM, Hamid M, Izadyar M (2011) Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family. Ann Haematol 90(3):349–351. https://doi.org/10.1007/s00277-010-1003-4

3. Marden FA, Putman CM, Grant JM, Greenberg J (2008) Moyamoya disease associated with hemoglobin Fairfax and beta-thalassemia. PediatrNeurol 38:130–132. https://doi.org/10.1016/j.pediatrneurol.2007.09.011

4. Dacie JV, Lewis SM (1995) Practical haematology, 8th edn. Churchill Livingstone, New York

5. Hb Var database. http://globin.cse.psu.edu/globin/hbvar . Last accessed on 02/04/2019