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Up to: Autosomal dominant disease · Intestinal polyposis syndrome

Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome

An autosomal dominant syndrome caused by pathogenic variants in the SMAD4 gene, characterized by the combined features of juvenile polyposis syndrome (JPS) and hereditary hemorrhagic telangiectasia (HHT). JPS features include multiple juvenile polyps in the gastrointestinal tract and an increased risk of gastrointestinal cancers. HHT features include arteriovenous malformations (AVMs) and telangiectasias.

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This condition has no sub-types.