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Syndrome in question.

Sheila Itamara Ferreira do Couto Meireles1, Sônia Maria Fonseca de Andrade1, Maria Fernanda Gomes1

  • 1Complexo Hospitalar Padre Bento de Guarulhos, Guarulhos, SP, Brazil.

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Summary
This summary is machine-generated.

Rendu-Osler-Weber Syndrome, or Hereditary Hemorrhagic Telangiectasia, is an inherited vascular disorder. This case report details a 64-year-old man diagnosed with this rare condition, highlighting its typical symptoms and complications.

Area of Science:

  • Genetics and rare diseases
  • Vascular medicine
  • Gastroenterology

Background:

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  • Rendu-Osler-Weber Syndrome (Hereditary Hemorrhagic Telangiectasia) is a rare autosomal dominant genetic disorder.
  • Characterized by mucocutaneous telangiectasias, recurrent epistaxis, and visceral arteriovenous malformations.
  • Associated complications can affect hematologic, neurologic, dermatologic, and gastrointestinal systems.