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Ophthalmic Genetics Volume 23, 2002 - Issue 4
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Research Article

Fanconi anemia and primary cataracts: first case

M. Merriman Department of Ophthalmology and Northern Regional Genetics Service, Auckland Hospital, Auckland, New Zealand
,
J. Mora Department of Ophthalmology and Northern Regional Genetics Service, Auckland Hospital, Auckland, New Zealand
&
J. McGaughran Department of Ophthalmology and Northern Regional Genetics Service, Auckland Hospital, Auckland, New Zealand
Pages 253-255 | Published online: 08 Jul 2009

References

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  • Alter BP. Fanconi's anaemia and its variability. Br J Haematol. 1993;85: 9–14. 3 Auerbach AD, Rogatteo A, Schroeder-Kurth TM. InternationalFanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity. Blood. 1989;73: 391–394.
  • Evans DGR, Rees HC, Spreadborough A, et al. Radial ray defects, renal ectopia, duodenal atresia, and hydrocephalus: the expanded spectrum for Fanconi anemia. Guth Dysmorphol. 1994;3: 200–206.
  • Giampietro PF, Adler-Brecher B, Verlander PC, Pavlakis SG, Davis JG, Auerbach AD. The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry. Paediatrics. 1993;91: iii6–1121.
  • Suh DW, Ruttum MS, Stuckenschneider BJ, Mieler WF, Kivlin JD. Ocular findings after bone marrow transplantation in a pediatric population. Ophthalmology. 1999;106:1564–1570.
  • Ng JS, Lam DS, Li CK, Chik KW, Cheng GP, Yuen PM, Tso MO. Ocular complications of pediatric bone marrow transplantation. Ophthalmology. 1999;106:16o–164.
  • Calissendorff BM, Lonnqvist B, el Azazi M. Cataract development in adult bone marrow transplant recipients. Acta Ophthalmol Scand. 1995;73:152–154.
  • Wajnrajch MP, Gertner JM, Huma Z, Popovic J, Lin K, Verlander PC, Batish SD, Giampietro PF, Davis JG, New MI, Auerbach AD. Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry. Pediatrics. 2001;107:744–754.

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