Loss of maternal allele in a child with myelodysplastic syndrome and monosomy 7

American Journal of Hematology

Volumn 62, Issue 1, 1999, Pages 49-51

  Aktas, Dilek ^a   Yenicesu, Idil ^a   Hicsonmez, Gonul ^a   Tuncbilek, Ergul ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

Monosomy 7; Myelodysplastic syndrome; Parental origin

Indexed keywords

DNA;

ACUTE MYELOBLASTIC LEUKEMIA; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 7Q; CHROMOSOME LOSS; FEMALE; HUMAN; HUMAN CELL; MONOSOMY 7; MYELODYSPLASTIC SYNDROME; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ALLELES; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 7; FATAL OUTCOME; FEMALE; HUMANS; LOSS OF HETEROZYGOSITY; MONOSOMY; MOSAICISM; MYELODYSPLASTIC SYNDROMES; POLYMERASE CHAIN REACTION;

EID: 0032832368     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8652(199909)62:1<49::AID-AJH8>3.0.CO;2-Y     Document Type: Article

References (23)

1. Martinez-Climent JA. Molecular cytogenetics of childhood hematological malignancies. Leukemia 1997;11:1999-2021.
2. Hann IM. Myelodysplastic syndromes. Archives of Disease in Childhood 1992;67:962-966.
3. Creutzing U, Cantu-Rajnoldi A, Ritter J, Romitti L, Odenwald E, Conter V, Riehm H, Masera G. Myelodysplastic syndrome in childhood. Report of 21 patients from Italy and West Germany. Am J Pediatr Haematol Oncol 1987;9:324-330.
4. Tuncer MA, Paglucia A, Hicsonmez G, Yetgin S, Ozsoylu S, Mufti GJ. Primary myelodysplastic syndrome in children: the clinical experience in 33 cases. Br J Haematol 1993;82:347-353.
5. Luna-Fineman S, Shannon KM, Lange BJ. Childhood monosomy 7: epidemiology, biology, and mechanistic implications. Blood 1995;85: 1985-1999.
6. Flactif M, Lai JL, Preudhomme C, Fenaux P. Fluorescence in situ hybridization improves the detection of monosomy 7 in myelodysplastic syndrome. Leukemia 1994;8:1012-1018.
7. Le Beau MM, Espinosa R, Davis EM, Eisenbart JD, Larson RA, Green ED. Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid disease. Blood 1996;88: 1930-1935.
8. Laver JH, Yusuf U, Cantu ES, Barredo JC, Holt LB, Abboud MR. Transient therapy-related myelodysplastic syndrome associated with monosomy 7 and 11q23 translocation. Leukemia 1997;11:448-455.
9. Maris JM, Wiersma SR, Mahgoub N, Thompson P, Geyer RJ, Hurwitz CG, Lange BJ, Shannon KM. Monosomy 7 myelodysplastic syndrome and other second malignant neoplasms in children with neurofibromatosis type 1. Cancer 1997;79:1438-1446.
10. Shannon KM, Turhan AG, Chang SSY, Bowcock AM, Rogers PCJ, Carroll WL, Cowan MJ, Glader BE, Eaves CJ, Eaves AC, Kan YW. Familial bone marrow monosomy 7. J Clin Invest 1989;84:984-989.
11. Johnson EJ, Scherer SW, Osborne L, Tsui LC, Oscier D, Mould S, Cotter FE. Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia. Blood 1996;87:3579-3586.
12. Johnson EJ, Cotter FE. Monosomy 7 and 7q- associated with myeloid malignancy. Blood 1997;11:46-55.
13. Liang H, Fairman J, Claxton DF, Nowell PC, Green ED, Nagarajan L. Molecular anatomy of chromosome 7q in myeloid neoplasms: Evidence for multiple critical loci. Proc Natl Acad Sci USA 1998;95: 3781-3785.
14. Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DAG, Gralnick HR, Sultan C. Proposals for the classification of the myelodysplastic syndrome. Br J Haematol 1982;51:189-199.
15. ISCN 1995. Guidelines for cancer cytogenetics. In: Mitelman F, ed. Supplement to an international system for human cytogenetic nomenclature. Basel: Karger, 1995.
16. Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nuc Acid Res 1996;16: 1215.
17. UTAH Marker Development Group. A collection of ordered tetranucleotide-repeat markers from the human genome. Am J Hum Genet 1995;57:619-628.
18. Scheffield VC, Weber JL, Buetow KH, Murray JC, Even DA, Wiles K. A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genomwide maps. Hum Mol Genet 1995;4:1837-1844.
19. Dib C, Fayre S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan J, Seboun E, Lathrop M, Gyapay G, Morissette & Weissenbach J. A comprehensive genetic map of the human genome based on 5264 microsatellites. Nature (London) 1996;380:152-154.
20. Aktas D, Ayhan A, Tuncbilek E, Ozdemir A, Uzunalimoglu B. No evidence for overexpression of the p53 protein and mutations in exons 4-9 of the p53 gene in a large family with adenomatous polyposis. Am J Gastroen 1998;93:1524-1526.
21. Katz F, Webb D, Gibbons B, Reeves B, McMahon C, Chessels J, Mitchell C. Possible evidence for genomic imprinting in childhood acute myeloblastic leukemia associated with monosomy for chromosome 7. Br J Haematol 1992;80:332-336.
22. Savage P, Frenck R, Paderange D, Emperor J, Shannon KM. Parental origins of chromosome 7 loss in childhood monosomy 7 syndrome. Leukemia 1994;8:485-489.
23. Shannon KM, Turhan AG, Rogers PCJ, Kan YW. Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7. Genomics 1992;14: 121-125.