hrp0098p1-212 | Adrenals and HPA Axis 3 | ESPE2024
Lekarev Oksana
, Sen Ginny
, Haider Mahroz
, Tang Fei
, Friedler Haley
, Chen Joy
, Lin-Su Karen
, Matos Dina
, Dessibourg Jackie
, Cheng Henry
, Roberts Eiry
, Chan Jean
, Jeha George
Introduction: Patients with classic congenital adrenal hyperplasia (CAH) require glucocorticoid (GC) therapy to replace cortisol insufficiency and reduce excess adrenal androgens, usually necessitating supraphysiologic GC doses. CAHtalog™, developed in partnership with CARES Foundation using the PicnicHealth platform, is a real-world US patient registry that characterizes the natural history of classic CAH. This study explored changes in health states ba...