进行性非综合征型聋家系临床表型及遗传学分析

合集下载
  1. 1、下载文档前请自行甄别文档内容的完整性,平台不提供额外的编辑、内容补充、找答案等附加服务。
  2. 2、"仅部分预览"的文档,不可在线预览部分如存在完整性等问题,可反馈申请退款(可完整预览的文档不适用该条件!)。
  3. 3、如文档侵犯您的权益,请联系客服反馈,我们会尽快为您处理(人工客服工作时间:9:00-18:30)。

进行性非综合征型聋家系临床表型及遗传学分析
李征玥;程静;卢宇;张旭;金占国;贾婧杰;袁慧军
【期刊名称】《听力学及言语疾病杂志》
【年(卷),期】2012(20)3
【摘要】目的分析一个连续五代常染色体显性遗传性非综合征型聋家系的临床表型及遗传学特征.方法对该耳聋家系成员进行病史采集、全身及听力学检查,绘制遗传图谱并进行遗传学特征分析.应用微卫星标记连锁分析方法及外显子序列分析对常染色体显性遗传(DFNA)23个基因的22个位点进行初步筛查.结果该耳聋家系共五代,现存家系成员44人,参与本研究的39人中耳聋患者16人,除1人为语前聋外,其他患者均表现为迟发性、渐进性听力下降,发病年龄介于14~40岁,早期以中频听力下降为主,逐渐累及高频,随着年龄的增长,呈全频听力下降.除DFNA5外,各DFNA位点连锁分析所得LOD值均<-2,提示该家系的致聋基因与这些位点均不连锁.对家系中2例患者和2例正常者DFNA5的所有外显子进行测序分析,未发现突变.结论该家系遗传方式符合常染色体显性遗传规律,表现为以中高频听力下降为主的感音神经性聋;对已知耳聋基因位点进行筛查,未发现明确的阳性位点;通过新一代测序技术进行全外显子组分析可能发现新的感音神经性聋致病基因.%Objective To study the phenotype and genetic characteristic of a five-generation Chinese family with autosomal dominant nonsyndromic hearing loss. Methods Members of this family were interviewed to identify their medical histories of hearing loss. Detailed audioiogy examination was performed and clinical data of this family was collected. A pedigree diagram was drawn according to the hereditary information. Prcscrccning of 22 DFNA
loci with 23 known DFNA genes by using microsatcllitc makers and linkage analysis and gene sequence analysis was performed. Results This family comprises 44 members. Thirty-nine family members anticipated showed prclingual onset. The other patients showed late-onset, progressive hearing loss, occurred between 14~40 years of age. The hearing loss began at the medium - frequency and whole frequencies became involved along with age. In addition to DFNA5, all other DFNA loci were less than -2, linkage analysis showed no linkages between pedigree gene and reported loci. Sequencing of the DFNA5 gene of 4 members (two patients and two normal) in this family found no mutation. Conclusion Pedigree analysis suggested an autosomal dominant inheritance pattern in this family. Positive linkage were not found in the known deafness loci we screened. The information should facilitate future gene identification by using next -generation sequencing technology for discovering of novel deafness genes.【总页数】5页(P201-205)
【作者】李征玥;程静;卢宇;张旭;金占国;贾婧杰;袁慧军
【作者单位】中国人民解放军总医院耳鼻喉研究所,北京,100853;中国人民解放军总医院耳鼻喉研究所,北京,100853;中国人民解放军总医院耳鼻喉研究所,北
京,100853;北京协和医院;中国人民解放军总医院耳鼻喉研究所,北京,100853;中国人民解放军总医院耳鼻喉研究所,北京,100853;中国人民解放军总医院耳鼻喉研究所,北京,100853
【正文语种】中文
【中图分类】R764.43
【相关文献】
1.一个常染色体显性遗传非综合征型聋家系的听力学及遗传学特征分析 [J], 牛志杰;蒋璐;梅凌云;冯永;陈红胜;贺楚峰;刘亚兰;王雪萍;刘畅
2.一个迟发性非综合征型常染色体显性遗传性聋家系表型特征及致病基因初步探讨[J], 王鸿涵;刘亚兰;卢焰梅;贺楚峰;冯永;王行炜;梅凌云;陈红胜;蒋璐;门美超;张华;李海波
3.非综合征型X连锁隐性遗传耳聋家系临床表型及遗传学特征分析 [J], 牛志杰;蒋璐;冯永;梅凌云;孙捷;陈红胜;贺楚峰;刘亚兰;王雪萍;文杰
4.线粒体基因组A1555G突变致非综合征性聋患者的临床表型分析 [J], 丁立才;刘玉和;马袆楠;钟贞;戚豫;柯肖枚
5.一个常染色体显性遗传非综合征型聋家系MYO6基因新致病性变异 [J], Tian Tao;Lu Yajie;Yao Jun;Cao Xin;Wei Qinjun;Li Qi
因版权原因,仅展示原文概要,查看原文内容请购买。

相关文档
最新文档