CGL2, also known as , is a rare autosomal recessive metabolic disorder.
: Unlike CGL Type 1, CGL2 is more frequently linked to neurological issues and cardiomyopathy. Other Potential Contexts CGL2.rar
: The lack of fat gives patients a highly defined, muscular look. CGL2, also known as , is a rare
: It is often associated with liver enlargement (steatosis), cardiomyopathy (heart muscle disease), and intellectual disability. also known as
: It is caused by mutations in the BSCL2 gene , which encodes the protein seipin . Seipin plays a critical role in lipid droplet formation and adipocyte (fat cell) maturation. Key Symptoms :