Describes two cases of the rare autosomal recessive disorder Familial chylomicronemia syndrome.
No takes yet. Share an insight, caveat, or question.
Reports of familial chylomicronemia syndrome aid rare-disease recognition; leaves open optimal management pending larger studies.
Chen et al. (2012) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: