单基因家族性高胆固醇血症样表型两家系报道
网络出版日期: 2015-02-27
基金资助
国家“十五”重大科技专项 (2002BA711A08-17) ;教育部科技基础平台建设(505015);甘肃省自然科学研究基金 (1308RJZA218, 2011y0217);国家留学基金委;横向课题基金(2012620111000212)
Report of two families of monogenic familial hypercholesterolemia like phenotype
Online published: 2015-02-27
Supported by
National Key Technology Research and Development Program of China during the “10th FiveYear” Plan,2002DA711A028-17; Science and Technology Infrastructure Platform of Ministry of Education, 505015;Natural Science Foundation of Gansu Province, 1308RJZA218, 2011y0217; China Scholarship Council; Horizontal Subject Foundation, 2012620111000212
何津春 , 周珊珊 , 李燕平 , 等 . 单基因家族性高胆固醇血症样表型两家系报道[J]. 上海交通大学学报(医学版), 2015 , 35(2) : 298 . DOI: 11.3969/j.issn.1674-8115.2015.02.029
Objective To report 2 families of monogenic familial hypercholesterolemia and their pedigree analysis and to improve the understanding of familial hypercholesterolemia. Methods The pedigree, biochemical results, and clinical data of 2 families of monogenic familial hypercholesterolemia were analyzed. Results There were 17 patients among 22 surviving members of two families. The onset of homozygous patients was earlier. Typical xanthoma was found among them. Their serum total cholesterol and low density lipoprotein cholesterol significantly increased. Triglycerides were normal. Electrocardiogram changes caused by the myocardial ischemia was discovered in the early stage. Conclusion The onset of this disease is early and can cause serious damages. Patients should undergo the early lipid-lowering therapy.
Key words: familial hypercholesterolemia; family; phenotype
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