Sudden Death in a 4-Year-Old Boy: A Near-Complete Occlusion of the Coronary Artery Caused by an Aggressive Low-Density Lipoprotein Receptor Mutation (W556R) in Homozygous Familial Hypercholesterolemia
- 31 January 2011
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 158 (1) , 167
- https://doi.org/10.1016/j.jpeds.2010.06.027
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Hyperlipidaemia in Paediatric PatientsDrug Safety, 2010
- Traitement d’une hypercholestérolémie familiale homozygote par LDL-aphérèse chez un enfant de 4 ansArchives de Pédiatrie, 2009
- Homozygous familial hypercholesterolemia: A novel point mutation (W556R) in a Turkish patientHuman Mutation, 2000
- Development of coronary heart disease in familial hypercholesterolemia.Circulation, 1989