The patient was a 68-year-old female with a confirmed genetic diagnosis of HHT (mutation in the ACVRL1 gene) with a strong family history of the disease. She had typical manifestations… Click to show full abstract
The patient was a 68-year-old female with a confirmed genetic diagnosis of HHT (mutation in the ACVRL1 gene) with a strong family history of the disease. She had typical manifestations of telangiec...
               
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