Two different karyotypes with 1q abnormalities in a patient with Fanconi anemia

Leukemia Research

Volumn 26, Issue 11, 2002, Pages 1047-1049

  Oliveira, Neide I S S ^a   Ribeiro, Enilze M S F ^a   Raimondi, Susana C ^b   Bittencourt, Marco A ^a   Pasquini, Ricardo ^a   Cavalli, Iglenir J ^a  

^a FEDERAL UNIVERSITY OF PARANÁ   (Brazil)

^b ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

Author keywords

1q; Deletion; Duplication; Fanconi anemia

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ARTICLE; BONE MARROW; CASE REPORT; CHILD; CHROMOSOME 1Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL FEATURE; CYTOGENETICS; FANCONI ANEMIA; HUMAN; KARYOTYPE; MALE; PRIORITY JOURNAL;

ACUTE DISEASE; BONE MARROW; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; FANCONI ANEMIA; HUMANS; KARYOTYPING; LEUKEMIA, MYELOID; MALE;

EID: 0036844159     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0145-2126(02)00038-3     Document Type: Article

References (13)

1. Fanconi G. Familial constitutional panmyelocytopathy. Fanconi's anemia (FA). I. Clinical aspects. Semin. Hematol. 4:1967;233-240.
2. Swift M.R. Fanconi's anaemia in the genetics of neoplasia. Nature. 230:1971;370-373.
3. Schroeder T.M., Tilgen D., Kruger J., Vogel F. Formal genetics of Fanconi's anemia. Hum. Genet. 32:1976;257-288.
4. Joenje H., Patel K.J. The emerging genetic and molecular basis of Fanconi anemia. Nature Rev. Genet. 2:2001;446-459.
5. Alter B.P., Caruso J.P., Drachtman R.A.et al. Fanconi anemia: myelodysplasia as a predictor of outcome. Cancer Genet. Cytogenet. 117:2000;125-131.
6. Raimondi SC, Mathew S, Pui C-H. Cytogenetics as a diagnostic aid for childhood hematologic disorders. In: Hanausek M, Walaszek Z, editors. Methods in molecular medicine, tumor markers protocols, vol. 14. Totowa, NJ: Humanae Press, 1998. p. 209-27.
7. Mitelman F, editor. ISCN, an international system for human cytogenetic nomenclature. Basel: S. Karger, 1995.
8. Carbone P., Barbata G., Mirto S., Granata G. Inherited aplastic anemia with abnormal clones in bone marrow and increased endoreduplication in peripheral lymphocytes. Cancer Genet. Cytogenet. 13:1984;259-266.
9. Maarek O., Jonveaux P., Le Coniat M.et al. Fanconi anemia and bone marrow clonal chromosome abnormalities. Leukemia. 10:1996;1700-1704.
10. Babu Rao V., Kerketta L., Ghosh K., Mohanty D.A. 46,XY,dup(1)(q21q32), add(11)(q23) karyotype in a case of Fanconi anemia. Leuk. Res. 25:2001;347-348.
11. Fundia A., Gorla N., Larripa I. Spontaneous chromosome aberrations in Fanconi's anemia patients are located at fragile sites and acute myeloid leukemia breakpoints. Hereditas. 120:1994;47-50.
12. Ferro M.T., Vazquez-mazariego Y., Ramiro S.et al. Triplication of 1q in Fanconi anemia. Cancer Genet. Cytogenet. 127:2001;38-41.
13. Nakamura Y., Komano H., Nakauchi H. Two alternative forms of cDNA encoding CD34. Exp. Hematol. 21:1993;236-242.