For over a decade, we've proudly given a voice to the voiceless in the rare community. Behind the Mystery collaborates with pharmaceutical companies, foundations, and patient advocacy groups to educate the public on rare and genetic diseases through our recurring segment on Lifetime Television. # 22q11.2 deletion syndrome / DiGeorge syndrome A Acromegaly Acute Hepatic Porphria Al Amyloidosis Alpha-1 (Understanding Alpha-1) Alpha-1 (Alpha-1 antitrypsin deficiency or AAT) Alport Syndrome Arginase I Deficiency ATTR Amyloidosis (1) ATTR Amyloidosis (2) ATTR Polyneuropahy Autosomal Dominant Hypocalcemia Type 1 (ADH1) Autosomal dominant polycystic kidney disease (ADPKD) B Blastic plasmacytoid dendritic cell neoplasm (BPDCN) C Cancer of Unknown Primary Castleman's Disease Chondrosarcoma Chronic Granulomatous Disease Chronic Thromboembolic Pulmonary Hypertension (CTEPH) Complex Regional Pain Syndrome Congenital Sucrase-isomaltase Deficiency Cooley's Anemia Cushing syndrome (1) Cushing syndrome
