Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia: Data from the Comprehensive HHT Outcomes Registry of the US (CHORUS)
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The authors aimed to characterize the clinical spectrum of hereditary hemorrhagic telangiectasia (HHT) using data from the Comprehensive HHT Outcomes Registry of the United States (CHORUS). Their findings reveal a significant delay in diagnosis, with many patients experiencing severe bleeding and complications, such as anemia and thromboembolism, highlighting the need for improved awareness and management of this condition. The study underscores the high burden of morbidity associated with HHT, emphasizing the importance of early detection and intervention.
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