Combined Juvenile Polyposis and Hereditary Hemorrhagic Telangiectasia

Abstract

The article presents a case study of a 27-year-old woman presented to the emergency room at Baylor University Medical Center at Dallas, Texas, complaining of symptoms including diarrhea, fatigue, and nausea. Her medical history showed intermittent small bowel obstructions and gastrointestinal bleeding requiring surgery. An overview of a diagnosis of combined autosomal dominant disorders juvenile polyposis (JP) and hereditary hemorrhagic telangiectasia (HHT) is presented.