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Brief ReportBrief Report

Acute Visual Loss as the Presenting Complaint of Hereditary Hemorrhagic Telangiectasia

Karissa L. Hackelton
The Journal of the American Board of Family Medicine November 2006, 19 (6) 637-640; DOI: https://doi.org/10.3122/jabfm.19.6.637
Karissa L. Hackelton
MD
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References

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    Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic Criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 2000; 91: 66–7.
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    Letteboer TGW, Mager JJ, Snijder, et al. Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia. J Med Genet 2006; 43: 371–7.
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    Shovlin CL, Letarte M. Hereditary Hemorrhagic Telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms. Thorax 1999; 54: 714–29.
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    Haitjema T, Westermann CJJ, Overtoom TTC, et al. Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease) new insights in pathogenesis, complications, and treatment. Arch Intern Med 1996; 156: 714–19.
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    Post MC, Letteboer TGW, Mager JJ, et al. A pulmonary right-to-left shunt in patients with hereditary hemorrhagic telangiectasia is associated with an increased prevalence of migraine. Chest 2005; 128: 2485–9.
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    Gallitelli M, Pasculli G, Fiore T, et al. Emergencies in hereditary haemorrhagic telangiectasia. Q J Med 2006; 99: 15–22.
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    Sobel D, Norman D. CNS Manifestations of hereditary hemorrhagic telangiectasia. AJNR 1984; 5: 569–73.
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    Moussouttas M, Fayad P, Rosenblatt M, et al. Pulmonary arteriovenous malformations: Cerebral ischemia and neurologic manifestations. Neurology 2000; 55: 959–64.
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    Fiorella ML, Ross DA, White RI, et al. Hereditary haemorrhagic telangiectasia: state of the art. Acta Otorhinolaryngol Ital 2004; 24: 330–6.
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    Georgiou T, Qureshi SH, Chakrabarty A, Noble BA. Choroidal telangiectasia in a patient with hereditary hemorrhagic telangiectasia. Eye 2002; 16: 92–4.
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    Davis DG, Smith JL. Retinal Involvement in hereditary hemorrhagic telangiectasia. Arch Ophthal 1971; 85: 618–23.
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    Knox FA, Frazer DG. Ophthalmic presentation of hereditary hemorrhagic telangiectasia. Eye 2004; 18: 947–9.
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    Brant AM, Schachat AP, White RI. Ocular manifestations in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease). Am J Ophthal 1989; 107: 642–6.
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    Yamakuchi M, Tanaka S, Tomosugi T, et al. Pulmonary arteriovenous fistula manifesting as amaurosis fugax. Neurol Med Chir (Tokyo) 2000; 40: 264–7.
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    Guttmacher AE, Marchuk DA, White RI. Hereditary hemorrhagic telangiectasia. N Engl J Med 1995; 333: 918–24.
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The Journal of the American Board of Family Medicine: 19 (6)
The Journal of the American Board of Family Medicine
Vol. 19, Issue 6
November-December 2006
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Acute Visual Loss as the Presenting Complaint of Hereditary Hemorrhagic Telangiectasia
Karissa L. Hackelton
The Journal of the American Board of Family Medicine Nov 2006, 19 (6) 637-640; DOI: 10.3122/jabfm.19.6.637

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Acute Visual Loss as the Presenting Complaint of Hereditary Hemorrhagic Telangiectasia
Karissa L. Hackelton
The Journal of the American Board of Family Medicine Nov 2006, 19 (6) 637-640; DOI: 10.3122/jabfm.19.6.637
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