Hereditary Hemorrhagic Telangiectasia: Diagnosis and Management

Hereditary Hemorrhagic Telangiectasia (HHT), or Rendu–Osler–Weber syndrome, is a dominantly inheritable rare disease with a prevalence of 1:5,000 – 10,000 people. The diagnosis of HHT, as a rare disease, follows the Curaçao Diagnostic Criteria: Nosebleeds (epistaxis), whether spontaneous or recurren...

Celý popis