Association of coronary heart disease with age-adjusted aortocoronary calcification in patients with familial hypercholesterolaemia

2000 ◽  
Vol 247 (4) ◽  
pp. 479-484 ◽  
Author(s):  
J. M. Jensen ◽  
L. U. Gerdes ◽  
H. K. Jensen ◽  
T. M. Christiansen ◽  
J. U. Brorholt-Petersen ◽  
...  
2020 ◽  
pp. 343-348
Author(s):  
Perry Elliott ◽  
Pier D. Lambiase ◽  
Dhavendra Kumar

Familial hypercholesterolaemia (FH) is an inborn error of metabolism that leads to accumulation of low-density lipoprotein cholesterol (LDL-C) particles in the blood and premature coronary artery atherosclerosis. This chapter covers the clinical criteria for the diagnosis of FH, the genetics that underpins the condition, cascade testing, premature coronary heart disease, and treatment methods.


2021 ◽  
pp. 981-1004
Author(s):  
Fredrik Karpe

This chapter begins with lipids and coronary heart disease, and the assessment of CVD risk in the patient. It describes primary hyperlipidaemias, polygenic and familial hypercholesterolaemia, familial hypertriglyceridaemia, and rare genetic hypertriglyceridaemias. Elevation of Lp(a), rare familial mixed dyslipidaemias, secondary hyperlipidaemias, and drug therapy are all covered.


2008 ◽  
Vol 29 (11) ◽  
pp. 1370-1376 ◽  
Author(s):  
Jeroen B. van der Net ◽  
Jeroen van Etten ◽  
Mojgan Yazdanpanah ◽  
Geesje M. Dallinga-Thie ◽  
John J.P. Kastelein ◽  
...  

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