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Bone Marrow Failure

Incidence of Fanconi anaemia in phenotypically normal aplastic anaemia patients in West Bengal

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References

  • Younghoon K, D’Andrea1 AD. Expanded roles of the Fanconi anemia pathway in preserving genomic stability. Genes Dev. 2010;24:1680–1694. doi: 10.1101/gad.1955310
  • Ketan J, Patel A, Joenjeb H. Fanconi anemia and DNA replication repair. Genes Dev. 2007;6:885–890.
  • Sagaseta IM, Molina J, Lezáun I, et al. Anemia de Fanconi. Consideraciones actuals. Anales Sis San Navarra. 2003;26:63–78.
  • Zen PRG, de Moraes FN, Rosa RFM, et al. Clinical characteristics of patients with Fanconi anemia. Rev Paul Pediatr. 2011;29:392–399. doi: 10.1590/S0103-05822011000300014
  • Katzenellenbogen RA, Carter JJ, Stern JE, et al. Skin and mucosal human papillomavirus sero prevalence in persons with Fanconi anemia. Clin Vaccine Immunol. 2015;22:413–420. doi: 10.1128/CVI.00665-14
  • Dokal I, Vulliamy T. Inherited aplastic anaemias/bone marrow failure syndromes. Blood Rev. 2008;22:141–153. doi: 10.1016/j.blre.2007.11.003
  • Jacquemont C, Taniguchi T. The Fanconi anemia pathway and ubiquitin. BMC Biochem. 2007;8:S10. doi: 10.1186/1471-2091-8-S1-S10
  • Alter BP, Giri N, Savage SA, et al. Cancer in dyskeratosis congenital. Blood. 2009;113:6549–6557. doi: 10.1182/blood-2008-12-192880
  • Shukla P, Ghosh K, Vundinti BR. Current and emerging therapeutic strategies for Fanconi anemia. Hugo J. 2012;6:1. doi: 10.1186/1877-6566-6-1
  • Eiler ME, Frohnmayer D, Frohnmayer L, et al. Fanconi anemia: guidelines for diagnosis and management. 4th ed. Eugene (OR): Fanconi Anemia Research Fund, Inc; 2014.
  • Tischkowitz MD, Hodgson SV. Fanconi anaemia. J Med Genet. 2003;40:1–10. doi: 10.1136/jmg.40.1.1
  • Rosenberg PS, Tamary H, Alter BP. How high are carrier frequencies of rare recessive syndromes? Contemporary estimates for Fanconi anemia in the United States and Israel. Am J Med Genet. 2011;155:1877–1883. doi: 10.1002/ajmg.a.34087
  • Sasaki MS, Tonomura A. A high susceptibility of Fanconi’s anemia to chromosome breakage by DNA cross-linking agents. Cancer Res. 1973;33:1829–1836.
  • Auerbach AD, Rogatko A, Schroeder-Kurth TM. International Fanconi anemia registry: relation of clinical symptoms to diepoxybutane sensitivity. Blood. 1989;73:391.
  • Auerbach AD. Fanconi anemia diagnosis and the diepoxybutane (DEB) test. Exp Hematol. 1993;21:731–733.
  • Meng CY, Noor PJ, Ismail A, et al. Chromosomal breakage test in the diagnosis of Fanconi anema in patients with aplastic anemia. Curr Res Med Med Sci. 2014;4:3–6.
  • Esmer C, Sánchez S, Ramos S, et al. Deb test for Fanconi anemia detection in patients with atypical phenotypes. Am J Med Genet. 2004;124A:35–39. doi: 10.1002/ajmg.a.20327
  • Auerbach AD. Diagnosis of Fanconi anemia by diepoxybutane analysis. Curr Protoc Hum Genet. 2016;85:8.7.1–8.7.17.
  • Pinto F O, Leblanc T, Chamousset D, et al. Diagnosis of Fanconi anemia in patients with bone marrow failure. Haematologica. 2009;94:487–495. doi: 10.3324/haematol.13592
  • Auerbach AD, Warburton D, Bloom AD, et al. Prenatal detection of the Fanconi anemia gene by cytogenetic methods. Am JHum Genet. 1979;31:77–81.
  • Oostra AB, Nieuwint AWM, Joenje H, et al. Diagnosis of Fanconi anemia: chromosomal breakage analysis. Hindawi Publishing Corporation. 2012;9.
  • Cirkovic S, Guc-Scekic M, Vujic D, et al. Diagnosis of Fanconi’s anemia by diepoxybutane analysis in children from Serbia. BJMG. 2011;14:65–70.
  • Aziz A, Mesba Chowdhury U, Khan R, et al. Fanconi anaemia – a rare case report. Bangladesh Med Res Counc Bull. 2016;42:1–5.
  • Varma N, Varma S, Marwaha RK, et al. Multiple constitutional aetiological factors in bone marrow failure syndrome (BMFS) patients from North India. Indian J Med Res. 2006;124:51–56.
  • Gupta V, Tripathi S, Singh TB, et al. A study of bone marrow failure syndrome in children. Indian J Med Sci. 2008;62:13–18. doi: 10.4103/0019-5359.38917
  • Jain D, Raina V, Fauzdar A, et al. Chromosomal breakage study in aplastic anemia patients in India. Asian J Med Sci. 2010;2:227–232.
  • Malla TM, Zargar MH, Dar FA, et al. Clastogen-induced chromosomal breakage analysis of suspected Fanconi’s anemia cases of Kashmir, North India. J Genet Syndr Gene. 2016;7:1–4. doi: 10.4172/2157-7412.1000295
  • Chowdhry M, Makroo RN, Srivastava P, et al. Clinicohematological correlation and chromosomal breakage analysis in suspected Fanconi anemia patients of India. Indian J Med Paediatr Oncol. 2014;35:21–25. doi: 10.4103/0971-5851.133706
  • Sinha S, Bhargava M. Fanconi anemia presenting as an “evolving” acute leukemia diagnostic challenges. Indian J Med Paediatr Oncol. 2013;34:305–308. doi: 10.4103/0971-5851.125251
  • Vijay Kumar BA, Biradar SG, Patil V, et al. Clinicohaematological profile of aplastic anaemia in BRIMS, teaching hospital, Bidar. IJBAR. 2014;5:10.
  • Athate UH, Rao SR, Kadam PR, et al. Fanconi’s anemia: a clinico-hematological and cytogenetic study. Indian Paediatrics. 1991;28:1003–1011.
  • Korgaonkar S, Ghosh K, Vundinti BR. Clinical, genetic and cytogenetic study of Fanconi anemia in an Indian population. Hematology. 2010;15:58–62. doi: 10.1179/102453310X12583347009531
  • Chakrabarti I, Saha A, Guha Mallick Sinha M, et al. Fanconi anemia with incidental haemoglobin E trait: the first reported case in literature. Indian J Hematol Blood Transfus. 2014;30:S111–S114. doi: 10.1007/s12288-013-0279-7
  • Shimamura A, de Oca RM, Svenson JL, et al. A novel diagnostic screen for defects in the Fanconi anemia pathway. Blood. 2002;100:4649–4654. doi: 10.1182/blood-2002-05-1399
  • Miglierina R, Coniat ML, Berger R. A simple diagnostic test for Fanconi anemia by flow cytometry. Anal Cell Pathol. 1991;3:111–118.

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