Fig. 2From: A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case reportPhotographs of serum samples of this patient (triglyceride 4.0 mmol/L) with clear appearance (A) and that of a patient with true hypertriglyceridemia (triglyceride 2.1 mmol/L) with turbid appearance (B)Back to article page