Homozygous familial hypercholesterolemia with severe involvement of the aortic valve-A sibling-controlled case study on the efficacy of lipoprotein apheresis.
Matthias GalianoJohanna HammersenKatja SauersteinHolger BlessingPetra RümmeleAriawan PurbojoMartin SchöberJulia MoosmannGunter RaffelsbauerAndreas HeibgesReinhard KlingelPublished in: Journal of clinical apheresis (2020)
LLT including LA should be initiated as early as possible following the diagnosis of hoFH with very high LDL-C levels. With the same genotype, the phenotype of hoFH can exhibit similar patterns but outcome is substantially related to treatment.