Macedonian Journal of Medical Sciences

نویسندگان

  • Vladimir Vukomanović
  • Milovan Matović
  • Vesna Ignjatović
  • Branislav Belić
چکیده

Hereditary hemorrhagic telangectasia (HHT) or Rendu-Osler-Weber syndrome, is a rare genetic disorder with autosomal dominance and variable penetrance. The typical findings of the disease are telangiectasias in skin and mucous membranes, and arteriovenous malformations presenting in the organs like lung, intestine, brain and liver. It is characterized by the classic triad of recurrent epistaxis, mucocutaneous telangiectasias and visceral hemorrhages, with familial occurrence.

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تاریخ انتشار 2014