中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2015年
16期
1222-1225
,共4页
陈园%郭艳英%吴岚%宋向欣%张洁%罗蕴之%王新玲
陳園%郭豔英%吳嵐%宋嚮訢%張潔%囉蘊之%王新玲
진완%곽염영%오람%송향흔%장길%라온지%왕신령
雄激素迟钝综合征%受体,雄激素%DNA突变分析%维吾尔族
雄激素遲鈍綜閤徵%受體,雄激素%DNA突變分析%維吾爾族
웅격소지둔종합정%수체,웅격소%DNA돌변분석%유오이족
Androgen-insensitivity syndrome%Receptors,androgen%DNA mutational analysis%Uygur
目的分析一个完全性雄激素不敏感综合征维吾尔族家系雄激素受体(AR)基因的突变及其临床特点,探讨该病的发病机制.方法针对该家系内2例临床拟诊为完全性雄激素不敏感综合征的男性假两性畸形患者,利用PCR扩增及DNA测序对AR基因的全部外显子及其剪切位点序列进行突变检测,并在家系及正常人群中验证所发现的突变.结果该家系2例患者临床表现均符合完全性雄激素不敏感综合征.先证者及其妹(社会性别女,染色体性别男)共2例均为AR基因c.2157G>A,p.W719X的无义突变,其母亲为该突变AR基因的携带者.该突变导致AR基因第4外显子2 157位碱基G突变为A,719位TGG密码子突变为TGA(终止密码子).该无义突变使AR蛋白截短202个氨基酸.正常人群中未发现该无义突变.结论AR基因W719X无义突变是该完全性雄激素不敏感综合征家系的致病突变.
目的分析一箇完全性雄激素不敏感綜閤徵維吾爾族傢繫雄激素受體(AR)基因的突變及其臨床特點,探討該病的髮病機製.方法針對該傢繫內2例臨床擬診為完全性雄激素不敏感綜閤徵的男性假兩性畸形患者,利用PCR擴增及DNA測序對AR基因的全部外顯子及其剪切位點序列進行突變檢測,併在傢繫及正常人群中驗證所髮現的突變.結果該傢繫2例患者臨床錶現均符閤完全性雄激素不敏感綜閤徵.先證者及其妹(社會性彆女,染色體性彆男)共2例均為AR基因c.2157G>A,p.W719X的無義突變,其母親為該突變AR基因的攜帶者.該突變導緻AR基因第4外顯子2 157位堿基G突變為A,719位TGG密碼子突變為TGA(終止密碼子).該無義突變使AR蛋白截短202箇氨基痠.正常人群中未髮現該無義突變.結論AR基因W719X無義突變是該完全性雄激素不敏感綜閤徵傢繫的緻病突變.
목적분석일개완전성웅격소불민감종합정유오이족가계웅격소수체(AR)기인적돌변급기림상특점,탐토해병적발병궤제.방법침대해가계내2례림상의진위완전성웅격소불민감종합정적남성가량성기형환자,이용PCR확증급DNA측서대AR기인적전부외현자급기전절위점서렬진행돌변검측,병재가계급정상인군중험증소발현적돌변.결과해가계2례환자림상표현균부합완전성웅격소불민감종합정.선증자급기매(사회성별녀,염색체성별남)공2례균위AR기인c.2157G>A,p.W719X적무의돌변,기모친위해돌변AR기인적휴대자.해돌변도치AR기인제4외현자2 157위감기G돌변위A,719위TGG밀마자돌변위TGA(종지밀마자).해무의돌변사AR단백절단202개안기산.정상인군중미발현해무의돌변.결론AR기인W719X무의돌변시해완전성웅격소불민감종합정가계적치병돌변.
Objective To identify the mutation of androgen receptor (AR) gene in a Uygur family with complete androgen insensitivity syndrome and elucidate its pathogenesis.Methods Two males with pseudohermaphroditism in this family were clinically diagnosed complete androgen insensitivity syndrome and by polymerase chain reaction (PCR) and DNA sequencing,we checked possible mutation of all exons and its splice site in AR gene.Two males with pseudohermaphroditism in this family were clinically diagnosed as complete androgen insensitivity syndrome and confirmed by PCR and DNA sequencing.And the possible mutations of all exons and splice sites in AR gene were examined.Results A proband and another family member had c.2157G > A,p.W719X nonsense mutation of AR gene and their mother was a mutation carrier of AR gene.Substitution (G-> A) at position 2 157 of exon 4 of AR resulted in mutation (TGG-> TGA) at codon 719 (termination codon).The nonsense mutation led to a truncation of 202 amino acids in AR protein.The mutations were absent in other family members.Conclusion The nonsense mutation at AR gene W719X,a confirmed cause of disease,is first-ever found in Chinese,especially Uygur population.