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https://pubmed.ncbi.nlm.nih.gov/38091604
In patients with Hereditary Hemorrhagic Telangiectasia (HHT), the presence of choroidal abnormalities is associated with the endoglin gene mutation, older age, corroborating retinal vascular changes, and increased systemic manifestations, although only a small proportion of patients with HHT undergo ophthalmic imaging.
