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A case with familial hypercholesterolemia complicated with severe systemic atherosclerosis intensively treated for more than 30 years
We present a case of a Japanese patient with familial hypercholesterolemia (FH) caused by a low-density lipoprotein (LDL) receptor gene mutation. A 47-year-old female was referred to our hospital due to her systemic xanthomatosis associated with elevated LDL-cholesterolemia (292 mg/dl). She was diag...
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| Udgivet i: | J Cardiol Cases |
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| Main Authors: | , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Japanese College of Cardiology
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7588487/ https://ncbi.nlm.nih.gov/pubmed/33133313 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jccase.2020.06.012 |
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