Alström syndrome (ALMS) is a rare genetic disorder characterized by a range of symptoms, including progressive hearing loss, vision problems, cardiomyopathy, and metabolic issues such as diabetes ...

Treatment includes managing symptoms and improving quality of life. Alström syndrome is a rare genetic disorder caused by ALMS1 gene mutations and affects multiple organs and systems. In addition ...

and Bardet-Biedl and Alström syndrome. It is in Phase 3 clinical trials for treating POMC or LEPR heterozygous deficiency obesities, steroid receptor coactivator 1 deficiency obesity, SH2B1 ...