- Six-year follow-up of a child with familial chylomicronemia syndrome: disease course and effectiveness of gemfibrozil treatment --case report and literature review
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Mustafa M, Almheiri M
- KMID: 2554684
- Ann Pediatr Endocrinol Metab.
- 2024 Apr;29(2):130-134.
- doi: 10.6065/apem.2346208.104
Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disease affecting lipoprotein metabolism. FCS is estimated to occur in 1 in 1–2 million individuals and can be diagnosed at any... -
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