Retinal vasculopathy in Fanconi anemia: A case report

Retina

Volumn 25, Issue 6, 2005, Pages 799-800

  Bahar, Irit ^a   Weinberger, Dov ^b   Kramer, Michal ^b   Axer Siegel, Ruth ^b  

^a RABIN MEDICAL CENTER   (Israel)

^b NONE

Author keywords

Cystoid macular edema (CME); Fanconi anemia; Peripheral occlusive

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CATARACT; CATARACT EXTRACTION; FANCONI ANEMIA; FEMALE; FLUORESCENCE ANGIOGRAPHY; HUMAN; PHACOEMULSIFICATION; RETINA BLOOD VESSEL OCCLUSION; RETINA HEMORRHAGE; RETINA MACULA CYSTOID EDEMA; RETINA VASCULITIS; VISUAL IMPAIRMENT;

ADULT; CATARACT; FANCONI ANEMIA; FEMALE; FLUORESCEIN ANGIOGRAPHY; HUMANS; LENS IMPLANTATION, INTRAOCULAR; MACULAR EDEMA, CYSTOID; PHACOEMULSIFICATION; RETINAL VASCULITIS; RETINAL VESSELS;

EID: 24344500178     PISSN: 0275004X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00006982-200509000-00023     Document Type: Article

References (3)

1. Gibbons B, Scott D, Hungerford JL, et al. Retinoblastoma in association with the chromosome breakage syndromes. Fanconi's anaemia and Bloom's syndrome: clinical and cytogenetic findings. Clin Genet 1995;47:311-317.
2. Merriman M, Mora J, McGaughram J. Fanconi anemia and primary cataracts: first case. Ophthalmic Genet 2002;23:253-255.
3. Niedermayer I, Reiche W, Graf N, Mestres P, Feiden W. Cerebroretinal vasculopathy and leukoencephalopathy mimicking a brain tumor. Report of two early-onset cases with Fanconi's anemia-like phenotypes suggesting an autosomal-recessive inheritance pattern. Clin Neuropathol 2000;19:285-295.