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- W2883146103 abstract "Familial hypercholesterolaemia (FH) is a genetic condition that results in elevated low-density lipoprotein (LDL) cholesterol (LDL-C) levels with consequent increased risk for premature cardiovascular disease events. Although it is considered an autosomal-dominant genetic condition, the underlying genetic causes of FH can be complex. Currently most guidelines rely on clinical criteria to diagnose FH. But this approach has some pitfalls. We present a patient who was not formally diagnosed with FH using commonly used and well-accepted clinical criteria but via genetic testing was found to have a mutation for this disorder. This case brings to fore the challenges clinicians face in diagnosing and managing such unusual cases optimally. Through this case report, we hope to stimulate a debate among clinicians as well as other stakeholders regarding the need to develop more efficient ways of selecting patients for genetic testing in response to elevated LDL levels." @default.
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- W2883146103 date "2018-07-19" @default.
- W2883146103 modified "2023-09-27" @default.
- W2883146103 title "Genetic testing for a patient with suspected familial hypercholesterolaemia" @default.
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- W2883146103 doi "https://doi.org/10.1136/bcr-2018-225259" @default.
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