Hematopoietic Reconstitution in a Patient with Fanconi's Anemia by Means of Umbilical-Cord Blood from an HLA-Identical Sibling

New England Journal of Medicine

Volumn 321, Issue 17, 1989, Pages 1174-1178

  Gluckman, Eliane ^a   Broxmeyer, Hal E ^a   Auerbach, Arleen D ^a   Friedman, Henry S ^a   Douglas, Gordon W ^a   Devergie, Agnès ^a   Esperou, Hélène ^a   Thierry, Dominique ^a   Socie, Gérard ^b   Lehn, Pierre ^b   Cooper, Scott ^b   English, Denis ^b   Kurtzberg, Joanne ^a   Bard, Judith ^a   Boyse, Edward A ^a  

^a SAINT LOUIS HOSPITAL   (France)

^b ROCKEFELLER UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AGE; CASE REPORT; FANCONI ANEMIA; FEMALE; HEMATOPOIESIS; HUMAN; MALE; NEWBORN; PRESCHOOL CHILD; PRIORITY JOURNAL; SIBLING; TRANSPLANTATION; UMBILICAL CORD BLOOD;

EID: 0024396816     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJM198910263211707     Document Type: Article

References (18)

1. Fanconi G. Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). I. Clinical aspects. Semin Hematol 1967; 4: 233–40.
2. Schroeder TM, Tilgen D, Kruger J, Vogel F. Formal genetics of Fanconi's anemia. Hum Genet 1976; 32: 257–88.
3. Auerbach AD, Rogatko A, Schroeder-Kurth TM. International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity. Blood 1989; 73: 391–6.
4. Auerbach AD, Wolman SR. Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens. Nature 1976; 261: 494–6.
5. Auerbach AD, Sagi M, Adler B. Fanconi anemia: prenatal diagnosis in 30 fetuses at risk. Pediatrics 1985; 76: 794–800.
6. Auerbach AD, Min Z, Ghosh R, et al. Clastogen-induced chromosomal breakage as a marker for first trimester prenatal diagnosis of Fanconi anemia. Hum Genet 1986; 73: 86–8.
7. Callaway C, Falcon C, Grant G, et al. HLA typing used with cultured amniotic and chorionic villus cells for early prenatal diagnosis or parentage testing without one parent's availability. Hum Immunol 1986; 16: 200–4.
8. Gluckman E, Devergie A, Dutreix J. Bone marrow transplantation for Fanconi's anemia. In: Schroeder-Kurth TM, Auerbach AD, Obe G, eds. Fanconi anemia: clinical, cytogenetic and experimental aspects. New York: Springer-Verlag, 1989:60–8.
9. Gluckman E, Devergie A, Schaison G, et al. Bone marrow transplantation in Fanconi anemia. Br J Haematol 1980; 45: 557–64.
10. Berger R, Bernheim A, Gluckman E, Gisselbrecht C. In vitro effect of cyclophosphamide metabolites on chromosomes of Fanconi anaemia patients. Br J Haematol 1980; 45: 565–8.
11. Gluckman E, Devergie A, Dutreix J. Radiosensitivity in Fanconi anaemia: application to the conditioning regimen for bone marrow transplantation. Br J Haematol 1983; 54: 431–40.
12. Broxmeyer HE, Douglas GW, Hangoc G, et al. Human umbilical cord blood as a potential source of transplantable hematopoietic stem/progenitor cells. Proc Natl Acad Sci USA 1989; 86: 3828–32.
13. Mann W, Venkatraj VS, Auerbach AD. Two hour hybridization using a new transfer membrane. Nucleic Acids Res 1989; 17: 5410.
14. Sale GE, Lemer KG, Barker EA, Shulman HM, Thomas ED. The skin biopsy in the diagnosis of acute graft-versus-host disease in man. Am J Pathol 1977; 89: 621–35.
15. Butturini A, Seeger RC, Gale RP. Recipient immune-competent T lymphocytes can survive intensive conditioning for bone marrow transplantation. Blood 1986; 68: 954–6.
16. Knowlton RG, Nelson CA, Brown VA, Page DC, Donis-Keller H. An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome. Nucleic Acids Res 1989; 17: 423–37.
17. Gale RP, Touraine J-L, Lucarelli G, eds. Fetal liver transplantation: proceedings of an international symposium held in Pesaro, Italy, September 29–October 1, 1984. Vol. 193. Progress in clinical and biological research. New York: Alan R. Liss, 1985:327–42.
18. Balner H. Bone marrow transplantation and other treatment after radiation injury. The Hague, Netherlands: Martinus Nijhoff, 1977:29–31.