Aplastic anemia in Nijmegen breakage syndrome [1]

Journal of Pediatrics

Volumn 141, Issue 5, 2002, Pages 742-

  Pasic, Srdjan ^a  

^a Mother and Child Health Institute   (Yugoslavia)

Author keywords

[No Author keywords available]

Indexed keywords

APLASTIC ANEMIA; CASE REPORT; CHILD; CLINICAL EXAMINATION; EPSTEIN BARR VIRUS; FEMALE; GENE DELETION; HUMAN; LETTER; LYMPHOCYTE COUNT; NIJMEGEN BREAKAGE SYNDROME; PRIORITY JOURNAL;

ANEMIA, APLASTIC; CHILD, PRESCHOOL; CHROMOSOME FRAGILITY; EPSTEIN-BARR VIRUS INFECTIONS; FATAL OUTCOME; FEMALE; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; LYMPHOMA, B-CELL; MICROCEPHALY; SYNDROME;

EID: 0036844327     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (5)

1. Resnik IB, Kondratenko I, Togoev O, Vasserman N, Shagina I, Evgrafov O, et al. Nijmegen breakage syndrome: Clinical characteristics and mutation analysis in eight unrelated Russian families. J Pediatr 2002:140;355-61.
2. Weemaes CR, Hustinx TW, Scheres JM, van Munster PJJ, Bakkeren JA, Taalman RD. A new chromosomal instability disorder: The Nijmegen breakage syndrome. Acta Paediatr Scand 1981;70:557-64.
3. International Nijmegen Breakage Syndrome Study Group. Nijmegen breakage syndrome. Arch Dis Child 2000;82:400-6.
4. Wegner RD, Chrzanowska KH, Sperling K, Strumm M. Ataxia-telangiectasia variants (Nijmegen breakage syndrome). In: Ochs HD, Smith CIE, Puck JM, eds. Primary Immunodeficiency Diseases a Molecular and Genetic Approach. Oxford (UK): Oxford University Press 1999; p. 324-34.
5. Seemeyer TA, Gross TG, Egeler RM, Pirrucello SJ, Davis JR, Kelly CM, et al. X-linked lymphoproliferative disease: Twenty-five years after discovery. Pediatr Res 1995;38:471-7.