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• W2886249975 abstract "To create awareness for the devastating influence of high cholesterol in familial hypercholesterolaemia (FH) on vessel walls. Persons with high LDL-C and a known mutation associated with FH have a 22-fold increase in CVD compared with those with a normal LDL-C and no genetic mutation. If the awareness of the need to diagnose and treat this genetic disorder at an early stage increases, great atherosclerotic impact later in life could be avoided. Every minute a child with heterozygous FH is born somewhere in the world and every day a child with homozygous FH is born. Recent findings include effective therapy on statins from the age of 6 years, with already normalization of the intima-media thickness within 2 years. Newer types of drugs, with the same safety profile and perhaps even more effective, will become available in childhood in the near future. Open for discussion will be whom to treat and with what type of treatment. Next generation sequencing will perhaps easily select those in need of treatment and those at risk of adverse effects. At the end of this review, statements and recommendations for children and adolescents with heterozygous FH are listed." @default.
• W2886249975 created "2018-08-22" @default.
• W2886249975 creator A5020436935 @default.
• W2886249975 date "2018-08-09" @default.
• W2886249975 modified "2023-10-18" @default.
• W2886249975 title "Lipid Screening, Action, and Follow-up in Children and Adolescents" @default.
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• W2886249975 doi "https://doi.org/10.1007/s11886-018-1014-7" @default.
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