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More than 80% of patients have mutations in one of the following genes (1): Endoglin (ENG) gene, which encodes a receptor for transforming growth factor beta-1 (TGF-1) and transforming growth factor beta-3 ACVRL1 gene, which encodes the activin receptor-like kinase (ALK1) MADH4 gene, which encodes SMAD4, a protein active in the TGF beta signaling pathway HHT is a disorder in which some blood vessels do not develop properly

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Archived from the original on December 20, 2019