Jun 25, 2019 · Familial hypercholesterolemia (FH) is an autosomal dominant disorder that causes severe elevations in total cholesterol and low-density lipoprotein cholesterol (LDLc). Xanthomas are noted commonly on the Achilles tendons and metacarpal phalangeal extensor tendons of the hands of patients with untreated FH.
2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk: The Task Force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and European Atherosclerosis Society (EAS).
Jul 02, 2014 · Methods. These guidelines were developed by Canadian experts in anxiety and related disorders through a consensus process. Data on the epidemiology, diagnosis, and treatment (psychological and pharmacological) were obtained through .
A number sign (#) is used with this entry because Smith-Lemli-Opitz syndrome (SLOS) is caused by homozygous or compound heterozygous mutation in the gene encoding sterol delta-7-reductase (DHCR7; 602858), which maps to chromosome 11q13. Description.
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