Hereditary hemorrhagic telangiectasia in a sudanese patient: A case report
- PMID: 35310313
- PMCID: PMC8918459
- DOI: 10.1002/ccr3.5585
Hereditary hemorrhagic telangiectasia in a sudanese patient: A case report
Abstract
(HHT) is a rare disorder affecting the skin and body's internal organs with a tendency for bleeding. We report a case of Sudanese 42-year-old with family history of HHT presented with recurrent epistaxis and telangiectasias.
Keywords: bleeding; colitis; epistaxis; hereditary; sudanese; telangiectasia.
© 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Conflict of interest statement
The authors report no conflict of interest.
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References
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- Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia telangiectasia (Rendu‐Osler‐Weber syndrome). Am J Med Genet. 2000;67:66‐67. - PubMed
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- Pahl KS, Choudhury A, Wusik K, et al. Applicability of the Curac¸ao criteria for the diagnosis of hereditary hemorrhagic telangiectasia in the pediatric population. J Pediatr. 2018;197:207‐213. - PubMed
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