Skip to main content
SpringerLink
Log in

Fanconi anemia

  • Clinical Briefs
  • Published:
The Indian Journal of Pediatrics Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

References

  1. Fanconi G. Familiare infantile perniziosaartige anamie (pernizioses blutbild and konstitution).Z. Kinderheilkunde 1927; 117: 257–259.

    Google Scholar 

  2. Auerback AD. Fanconi anemia diagnosis and the diepoxybutane (DEB) test.Exp Hematol 1993; 21: 731–735.

    Google Scholar 

  3. Auerbach AD, Rogatko A, Schroeder-Kurth TM. International Fanconi anemia registry: relation of clinical symptoms to diepoxybutane sensitivity.Blood 1989; 73: 391–396.

    PubMed  CAS  Google Scholar 

  4. Dosik H, Hsu LY, Todaro GJet al. Leukemia in Fanconi anemia: cytogenetic and tumor virus susceptibility studies.Blood 1970; 36: 341–347.

    PubMed  CAS  Google Scholar 

  5. Altay C, Sevgi Y, Pirnar T. Fanconi anemia in offspring of patient with congenital radial and carpal hypoplasia.N Engl J Med 1975; 293: 151–152.

    PubMed  CAS  Google Scholar 

  6. Bloom GE, Warner S, Gerald PS, Diamond LK. Chromosome abnormalitites in constitutional aplastic anemia.New Engl J Med 1966; 274: 8–14.

    Article  PubMed  CAS  Google Scholar 

  7. Liu JM, Auerbach AD, Young NS. Fanconi anemia presenting unexpectedly in an adult kindred with no dysmorphic features.Am J Med 1991; 91: 555.

    Article  PubMed  CAS  Google Scholar 

  8. Brown G, Buckton WM, McLean MS. Quantitative studies of chromosome aberrations in man following acute and chronic exposure to X-rays and gamma rays.Lancet 1965; 1: 1239–1242.

    Article  Google Scholar 

  9. Alter BP. Fanconi anemia and its variability.Br J Hematol 1993; 85: 9–13.

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Department of Hematology, Post Graduate Institute of Medical Education and Research, 160 012, Chandigarh

    Sabita Basu (Assistant Professor), Gurjeevan Garewal, S. Kaur, Amita Trehan & R. K. Marwaha

  2. Department of Pediatrics, Post Graduate Institute of Medical Education and Research, Chandigarh

    Sabita Basu (Assistant Professor), Gurjeevan Garewal, S. Kaur, Amita Trehan & R. K. Marwaha

Authors
  1. Sabita Basu
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Gurjeevan Garewal
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. S. Kaur
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Amita Trehan
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. R. K. Marwaha
    View author publications

    You can also search for this author in PubMed Google Scholar

Additional information

Editor’s note: Fanconi’s anemia is an autosomal recessive disorder. Diagnosis should be confirmed by DEB test (ref 2). Risk of recurrence is 25%. Prenatal diagnosis has been successfully done in one case at Genetics Unit, AIIMS, New Delhi.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Basu, S., Garewal, G., Kaur, S. et al. Fanconi anemia. Indian J Pediatr 63, 399–402 (1996). https://doi.org/10.1007/BF02751539

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02751539

Keywords

Search

Navigation