A 28-year-old female patient first diagnosed with mid-aortic syndrome

Abstract The mid-aortic syndrome is an uncommon condition characterized by segmental narrowing of the proximal abdominal aorta and ostial stenosis of renal and visceral branches. This syndrome is an unusual entity and mostly diagnosed in children and young adults. In this case report we describe a female patient who was first diagnosed with mid-aortic syndrome at the age of 28 years.