检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:王冠雄 刘丽婷 高阳 吕明荣[1,2,3] 吴欢 贺小进[1,2,3] Wang Guanxiong;Liu Liting;Gao Yang;Lyu Mingrong;Wu Huan;He Xiaojin(Reproductive Medicine Center of Obstetrics and Gynecology,the First Affiliated Hospital of Anhui Medical University,Hefei,Anhui 230022,China;NHC Key Laboratory of Study on Abnormal Gametes and Reproductive Tract,Anhui Medical University,Hefei,Anhui 230022,China;Key Laboratory of Population Health Across Life Cycle,Anhui Medical University,Hefei,Anhui 230022,China)
机构地区:[1]安徽医科大学第一附属医院妇产科生殖医学中心,合肥230022 [2]国家卫生健康委配子及生殖道异常研究重点实验室,合肥230022 [3]出生人口健康教育部重点实验室,合肥230022
出 处:《中华医学遗传学杂志》2023年第4期458-461,共4页Chinese Journal of Medical Genetics
基 金:国家重点研发计划(2019YFC1005106)。
摘 要:目的探讨1例家族性高胆固醇血症(FH)患者LDLR基因的变异特点,为其临床诊断与遗传咨询提供依据。方法选取2020年6月于安徽医科大学第一附属医院生殖中心就诊的1例FH患者为研究对象。收集患者的临床资料,应用全外显子组测序(WES)对患者进行基因检测,应用Sanger测序对候选变异进行家系验证,查阅UCSC数据库进行变异位点保守性分析。结果患者的临床表现为血清总胆固醇水平升高,其中低密度脂蛋白胆固醇显著升高。WES结果显示患者LDLR基因存在c.2344A>T(p.Lys782*)杂合变异,既往未见报道。Sanger测序验证该变异为父源性,患者父亲LDLR基因存在c.2344A>T(p.Lys782*)杂合变异,患者母亲该位点为野生型。查询UCSC数据库提示该变异位点高度保守。结论LDLR基因c.2344A>T杂合变异可能为该FH患者的遗传学病因。本研究为该家系的遗传咨询和产前诊断提供了依据。Objective To analyze variant of LDLR gene in a patient with familial hypercholesterolemia(FH)in order to provide a basis for the clinical diagnosis and genetic counseling.Methods A patient who had visited the Reproductive Medicine Center of the First Affiliated Hospital of Anhui Medical University in June 2020 was selected as the study subject.Clinical data of the patient was collected.Whole exome sequencing(WES)was applied to the patient.Candidate variant was verified by Sanger sequencing.Conservation of the variant site was analyzed by searching the UCSC database.Results The total cholesterol level of the patient was increased,especially low density lipoprotein cholesterol.A heterozygous c.2344A>T(p.Lys782*)variant was detected in the LDLR gene.Sanger sequencing confirmed that the variant was inherited from the father.Conclusion The heterozygous c.2344A>T(p.Lys782*)variant of the LDLR gene probably underlay the FH in this patient.Above finding has provided a basis for genetic counseling and prenatal diagnosis for this family.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.3