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致病性 ABCG5 基因突变导致的严重高胆固醇血症患儿。

Children with Severe Hypercholesterolemia Caused by a Pathogenic Mutation in ABCG5.

机构信息

Department of Cardiology, Kanazawa University Graduate School of Medicine, Japan.

出版信息

Intern Med. 2023 Jan 15;62(2):251-259. doi: 10.2169/internalmedicine.0050-22. Epub 2022 Jun 14.

Abstract

We herein present a case series of hypercholesterolemia caused by a pathogenic mutation in the ATP-binding cassette sub-family G member 5 (ABCG5). Three unrelated infantile patients who were breastfed and had extremely elevated low-density lipoprotein (LDL) cholesterol levels were referred to our hospital. Their LDL cholesterol levels decreased significantly after weaning. Panel sequencing revealed a pathogenic mutation in ABCG5 in each patient. An 8-year-old girl was also referred due to suspected familial hypercholesterolemia. Panel sequencing revealed a pathogenic mutation in ABCG5. A cholesterol-reduced diet alone significantly reduced the LDL cholesterol levels. Moreover, the administration of ezetimibe was found to be beneficial.

摘要

我们在此介绍了一组由 ATP 结合盒亚家族 G 成员 5(ABCG5)中的致病性突变引起的高胆固醇血症病例。3 名非相关的婴儿患者均为母乳喂养,且低密度脂蛋白(LDL)胆固醇水平极高,他们被转至我院。他们的 LDL 胆固醇水平在断奶后显著下降。基因测序显示每位患者的 ABCG5 中均存在致病性突变。一名 8 岁女孩也因疑似家族性高胆固醇血症被转至我院。基因测序显示 ABCG5 中存在致病性突变。单独采用降胆固醇饮食显著降低了 LDL 胆固醇水平。此外,发现依折麦布的使用也有益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8673/9908398/10ffb3625d36/1349-7235-62-0251-g001.jpg

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