Hereditary Hemorrhagic Telangiectasia (HHT, Osler–Weber–Rendu disease) — Symptoms and Diagnosis

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چکیده

Hereditary hemorrhagic telangiectasia (HHT) or Osler-Weber-Rendu-Disease (OWRD) is a rare autosomal dominant disorder that affects blood vessels and consequently multiple systems resulting in a tendency to bleed. Also known as vascular dysplasia, the condition is more or less diagnosed clinically and has a variable prognosis depending on prompt recognition and severity. However, there is no cure. This article will throw light on clinical features of the disease as well as its diagnosis to aid in identification and management.

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Hereditary Hemorrhagic Telangiectasia (HHT, Osler–Weber–Rendu disease) — Symptoms and Diagnosis

Hereditary hemorrhagic telangiectasia (HHT) or Osler-Weber-Rendu-Disease (OWRD) is a rare autosomal dominant disorder that affects blood vessels and consequently multiple systems resulting in a tendency to bleed. Also known as vascular dysplasia, the condition is more or less diagnosed clinically and has a variable prognosis depending on prompt recognition and severity. However, there is no cur...

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Anesthetic considerations for the patient with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome).

Hereditary hemorrhagic telangiectasia (HHT), Osler-Weber-Rendu Syndrome, is an uncommon disease but may be present in many people who remain undiagnosed. It is an autosomal dominant disorder characterized by multiple arteriovenous malformations (AVMs) and telangiectases that affect multiple organ systems. Hereditary hemorrhagic telangiectasia patients have a propensity for bleeding, especially ...

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Osler-Weber-Rendu syndrome.

Osler–Weber–Rendu syndrome, also known as Hereditary Hemorrhagic Telangiectasia (HHT), is an autosomal dominant disorder. Telangiectasias and Arterio-Venous Malformations (AVMs) are vascular lesions present in HHT, most commonly causing epistaxis and gastrointestinal bleeding. While epistaxis presents as early as childhood, the gastrointestinal manifestations of HHT develop with increasing age.

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Hereditary Hemorrhagic Telangiectasia: Presenting with Epistaxis

Osler-Weber-Rendu disease (OWRD) or Hereditary Hemorrhagic Telangiectasia (HHT) is a rare autosomal dominant disorder that causes muco-cutanesous and visceral vascular dysplasia and results in increased tendency for bleeding [1-4]. Patients with HHT may present with variety of symptoms and management differs accordingly. Epistaxis is the most common symptom of HHT and mucocutaneous telangiectas...

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Hereditary hemorrhagic telangiectasia or Rendu-Osler-Weber syndrome in the same family.

The authors present the case of three patients from the same family in whom hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber syndrome was diagnosed. The disease is rare and occurs with multiple telangiectases of the skin and mucosa, and pulmonary arteriovenous fistulae. The clinical status of our patients included multiple telangiectases of the skin and mucosa, recurrent epistax...

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تاریخ انتشار 2017