Purpose—Much has transpired since the last scientific statement on pediatric stroke was
published 10 years ago. Although stroke has long been recognized as an adult health …

This guideline presents recommendations for the management of patients with hereditary
gastrointestinal cancer syndromes. The initial assessment is the collection of a family history …

Description: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant
disease with an estimated prevalence of 1 in 5000 that is characterized by the presence of …

Vascular disorders of the liver, although affecting less than 5/10,000 patients, collectively
account for a number of rare conditions that represent an important health problem …

The gastrointestinal hamartomatous polyposis syndromes are rare, autosomal dominant
disorders associated with an increased risk of benign and malignant intestinal and …

Disorders of the mesenteric, portal, and hepatic veins and mesenteric and hepatic arteries
have important clinical consequences and may lead to acute liver failure, chronic liver …

An arteriovenous malformation is a tangle of dysplastic vessels (nidus) fed by arteries and
drained by veins without intervening capillaries, forming a high-flow, low-resistance shunt …

Hereditary haemorrhagic telangiectasia, inherited as an autosomal dominant trait, affects
approximately 1 in 5000 people. The abnormal vascular structures in HHT result from …

Context The only treatment available to restore normal cardiac output in patients with
hereditary hemorrhagic telangiectasia (HHT) and cardiac failure is liver transplant. Anti …

Abstract Abstract Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) is
a disorder of development of the vasculature characterized by telangiectases and …