: Patients have a near-total lack of body fat from birth or early infancy.
: Common complications include severe insulin resistance, early-onset diabetes mellitus, and high levels of triglycerides.
CGL2, also known as , is a rare autosomal recessive metabolic disorder.
: The lack of fat gives patients a highly defined, muscular look.
If you are referring to a file for a specific technical application, "CGL2" may also relate to:
: It is often associated with liver enlargement (steatosis), cardiomyopathy (heart muscle disease), and intellectual disability.
: Unlike CGL Type 1, CGL2 is more frequently linked to neurological issues and cardiomyopathy. Other Potential Contexts
