A case report of heterozygous familial hypercholesterolaemia with LDLR gene mutation complicated by premature coronary artery disease detected in primary care

A case report of heterozygous familial hypercholesterolaemia with LDLR gene mutation complicated by premature coronary artery disease detected in primary care

Background Familial hypercholesterolaemia (FH) is an autosomal dominant genetic condition predominantly caused by the low-density lipoprotein receptor (LDLR) gene mutation Case summary This is the case of a 54-year-old Malay woman with genetically confirmed FH complicated by premature coronary arter...

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Bibliographic Details
Published in:European Heart Journal - Case Reports
Main Author: Abdul-Halim M.A.Z.; Abdul-Hamid H.; Baharudin N.; Mohamed-Yassin M.-S.; Kasim S.S.; Nawawi H.; Qureshi N.; Ramli A.S.
Format: Article
Language:English
Published: Oxford University Press 2024
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85184814595&doi=10.1093%2fehjcr%2fytae039&partnerID=40&md5=f88b215a469ecdc10d50408f16a6d580

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https://www.scopus.com/inward/record.uri?eid=2-s2.0-85184814595&doi=10.1093%2fehjcr%2fytae039&partnerID=40&md5=f88b215a469ecdc10d50408f16a6d580

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