Airing weekdays at 7:30 A.M. on

Airing weekdays at 7:30 A.M. on

Imagine: A rare disease that’s rarely diagnosed because it mimics so many other diseases. We’re talking about Alpha-1 antitrypsin deficiency or AAT, a hereditary condition that may cause lung disease and liver disease. Dr. Kyle Hogarth, a pulmonologist at the University of Chicago, joins us to discuss the disease. Who’s at risk of getting this condition? What tests determine if you have it? And what lifestyle changes can help patients cope with this disease? We have lots of insight.

Behind the Mystery is a special segment dedicated to revolutionizing the way the health care system works for those suffering from a rare and genetic disorder.

Behind the Mystery takes a closer look at one of the two types of Polycystic Kidney disease. Autosomal Dominant Polycystic Kidney Disease, or ADPKD, is a rare, genetic condition.

Behind the Mystery takes a closer look at Blastic Plasmacytoid Dendritic Cell Neoplasm, a rare disease that is often misdiagnosed and affects at least 500 to 1,000 patients each year in the U.S.

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