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...
| الحاوية / القاعدة: | European Heart Journal - Case Reports |
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| المؤلف الرئيسي: | |
| التنسيق: | مقال |
| اللغة: | English |
| منشور في: |
Oxford University Press
2024
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| الوصول للمادة أونلاين: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85184814595&doi=10.1093%2fehjcr%2fytae039&partnerID=40&md5=f88b215a469ecdc10d50408f16a6d580 |