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...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
الحاوية / القاعدة:J Cardiol Cases
المؤلفون الرئيسيون: Nishikawa, Tetsuo, Tada, Hayato, Nakagawa-Kamiya, Tamami, Niwa, Satoru, Yoshida, Shohei, Mori, Mika, Sakata, Kenji, Nohara, Atsushi, Higashikata, Toshinori, Kato, Hiroki, Ino, Kenji, Takemura, Hirofumi, Takamura, Masayuki, Kawashiri, Masa-aki
التنسيق: Artigo
اللغة:Inglês
منشور في: Japanese College of Cardiology 2020
الموضوعات:
Case Report
الوصول للمادة أونلاين: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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