priklijavai
Priklijavai is a rare genetic disorder characterized by a failure of epidermal and corneal lipid metabolism. It is often associated with erythema dyschromicum perstans, a skin condition marked by the appearance of discolored patches on the skin. The disorder is typically inherited in an autosomal recessive pattern.
Individuals affected by priklijavai may experience a range of symptoms, including skin lesions, sensitivity to light,
The underlying cause of priklijavai is related to a deficiency of the enzyme acyl-CoA:diacylglycerol acyltransferase 2,
Due to its rarity and limited understanding, research into priklijavai remains limited. However, advancements in genetic