Fanconi’s Anemia Effect or Sickle Cell Anemia Effect: That is the Question
作者： Sule Unal , David H.K. Chui , Fatma Gumruk
DOI: 10.3109/03630269.2015.1041036
关键词:
摘要: AbstractA 16-year-old boy who was diagnosed to have sickle cell anemia referred our center. The parental consanguinity, growth retardation and dysmorphic features prompted a search for possible Fanconi’s Anemia (FA). diepoxybutane (DEB) test positive, confirming FA. interaction of both diseases might account his relatively mild phenotype in terms (or Hb S, HBB: c.20A > T) high F level that be related concomitant FA, may caused milder anemia, whereas nitric oxide (NO) depletion as consequence delay the bone marrow failure
informahealthcare.com参考文章(20)
D Schindler, H Hoehn, Fanconi anemia mutation causes cellular susceptibility to ambient oxygen. American Journal of Human Genetics. ,vol. 43, pp. 429- 435 ,(1988)
Rosatelli Mc, Oner R, Cao A, Moi B, Leoni Gb, Atzori G, Altay C, Beta-globin haplotype and XmnI polymorphism at position G (gamma)-158 and HbF production in Fanconi's anemia. Haematologica. ,vol. 77, pp. 106- 109 ,(1992)
João Ricardo Friedrisch, Daniel Prá, Sharbel Weidner Maluf, Christina Matzembacher Bittar, Michelle Mergener, Tiago Pollo, Michele Kayser, Maria Aparecida Lima da Silva, João Antonio Pêgas Henriques, Lucia Mariano da Rocha Silla, DNA damage in blood leukocytes of individuals with sickle cell disease treated with hydroxyurea. Mutation Research-genetic Toxicology and Environmental Mutagenesis. ,vol. 649, pp. 213- 220 ,(2008) , 10.1016/J.MRGENTOX.2007.09.005
Maria Plonczynski, Maria Stella Figueiredo, Martin H. Steinberg, Fetal Hemoglobin in Sickle Cell Anemia: Examination of Phylogenetically Conserved Sequences Within the Locus Control Region but Outside the Cores of Hypersensitive Sites 2 and 3☆☆☆ Blood Cells Molecules and Diseases. ,vol. 23, pp. 188- 200 ,(1997) , 10.1006/BCMD.1997.0136
Idowu Akinsheye, Abdulrahman Alsultan, Nadia Solovieff, Duyen Ngo, Clinton T. Baldwin, Paola Sebastiani, David H. K. Chui, Martin H. Steinberg, Fetal hemoglobin in sickle cell anemia Blood. ,vol. 118, pp. 19- 27 ,(2011) , 10.1182/BLOOD-2011-03-325258
Lars U. W. Müller, Michael D. Milsom, Chad E. Harris, Rutesh Vyas, Kristina M. Brumme, Kalindi Parmar, Lisa A. Moreau, Axel Schambach, In-Hyun Park, Wendy B. London, Kelly Strait, Thorsten Schlaeger, Alexander L. DeVine, Elke Grassman, Alan D'Andrea, George Q. Daley, David A. Williams, Overcoming Reprogramming Resistance of Fanconi Anemia Cells Blood. ,vol. 119, pp. 5449- 5457 ,(2012) , 10.1182/BLOOD-2012-02-408674
Juan I. Garaycoechea, K. J. Patel, Why does the bone marrow fail in Fanconi anemia Blood. ,vol. 123, pp. 26- 34 ,(2014) , 10.1182/BLOOD-2013-09-427740
Gregory J. Kato, Mark T. Gladwin, Martin H. Steinberg, Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes Blood Reviews. ,vol. 21, pp. 37- 47 ,(2007) , 10.1016/J.BLRE.2006.07.001
Subhashini Bolisetty, Edgar Jaimes, Mitochondria and reactive oxygen species: physiology and pathophysiology. International Journal of Molecular Sciences. ,vol. 14, pp. 6306- 6344 ,(2013) , 10.3390/IJMS14036306
Fatma Gumruk, Betul Tavil, Gunay Balta, Selma Unal, Aytemiz Gurgey, Significance of fetal hemoglobin values in detection of heterozygotes in fanconi anemia: reevaluation of fetal hemoglobin values by a sensitive method. Journal of Pediatric Hematology Oncology. ,vol. 30, pp. 896- 899 ,(2008) , 10.1097/MPH.0B013E3181833835