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Kumari, A

Case report and literature review: catastrophic embolism following cosmetic injection of autologous fat in the face

Familial chylomicronemia syndrome is a rare genetic disorder estimated to affect 1 to 2 individuals per million and characterized by hypertriglyceridemia, which is caused by mutations in LPL or genes that regulate LPL function which include but are not limited to APOC2, APOA5, GPIHBP1, and lipase maturation factor 1 (LMF1) [19,20]

The evidence available does not conclusively indicate which specific antioxidants or treatment regimens are most effective in enhancing sperm parameters and increasing pregnancy rates [243]