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Familial hyperchlolesterolaemia : a monogenic cause of early CHD

Author: Steve E Humphries
Publisher: London : Henry Stewart Talks, 2008.
Series: Henry Stewart talks., Biomedical & life sciences collection., Genetics of cardiovascular disease : genetic interactions in a multifactorial disease and toxicity.
Edition/Format:   eVideo : Clipart/images/graphics : EnglishView all editions and formats
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Material Type: Clipart/images/graphics, Internet resource, Videorecording
Document Type: Internet Resource, Computer File, Visual material
All Authors / Contributors: Steve E Humphries
OCLC Number: 431950395
Notes: Animated audio-visual presentation with synchronized narration.
Title from title frames.
Description: 1 streaming video file (50 min.).
Contents: Clinical diagnostic criteria --
Prevalence in UK --
Effects of statins on cholesterol and CHD risk lowering --
The 3 genes where mutations cause FH (LDLR, APOB, PCSK9) --
Clinical Genetics Diagnostic service for FH and examples in families --
Cascade testing for FH patients using LDL cholesterol levels --
The Overlap problem --
The Simon Broome FH register project and the high risk of early CHD in those with an LDLR and PCSK9 mutation --
The LDLR mutation database --
Ethical issues about genetic testing for FH --
Clinical questions in the management of FH --
FH testing and insurance.
Series Title: Henry Stewart talks., Biomedical & life sciences collection., Genetics of cardiovascular disease : genetic interactions in a multifactorial disease and toxicity.
Responsibility: Steve Humphries.
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