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脆性X综合征的直接分子诊断经验。

Experience with direct molecular diagnosis of fragile X.

作者信息

Mulley J C, Yu S, Gedeon A K, Donnelly A, Turner G, Loesch D, Chapman C J, Gardner R J, Richards R I, Sutherland G R

机构信息

Department of Cytogenetics and Molecular Genetics, Adelaide Children's Hospital, South Australia.

出版信息

J Med Genet. 1992 Jun;29(6):368-74. doi: 10.1136/jmg.29.6.368.

Abstract

The utility of the pfxa3 probe for direct molecular diagnosis of the fragile X (FRAXA) has been established. This probe detects amplification of an unstable DNA element consisting of variable length CCG repeats. The size of the amplified fragment is correlated with phenotype and was determined using PstI digested DNA in family members. In 35 families with the fragile X, there was correspondence in 183 cases between the presence of an amplified unstable element and the presence of the fragile X chromosome independently determined by cytogenetics, position in the pedigree, or linked DNA markers flanking the fragile X. There was also correspondence in 124 cases between the presence of the normal 1.0 kb PstI fragment and absence of the fragile X chromosome independently determined by linked flanking markers. Six additional families considered to be isolated cases of 'fragile X' had been diagnosed before recognition of FRAXD. The pfxa3 probe confirmed the cytogenetic diagnosis in three families, the other three being rediagnosed as non-fragile X. A further two families had consistent expression of a different folate sensitive fragile site, FRAXE, close to FRAXA but not associated with fragile X syndrome and not detectable with the pfxa3 probe. Subsequent referrals were received from additional family members or from members of new families for whom carrier status had not been predetermined by linked markers. Direct pfxa3 diagnosis for the 135 females within these 222 additional cases was confirmed by dosage analysis with the control probe pS8.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

pfxa3探针用于脆性X(FRAXA)直接分子诊断的效用已得到确立。该探针可检测由可变长度CCG重复序列组成的不稳定DNA元件的扩增。扩增片段的大小与表型相关,并通过对家庭成员的PstI消化DNA进行测定。在35个脆性X家庭中,183例中扩增不稳定元件的存在与通过细胞遗传学、家系位置或脆性X侧翼连锁DNA标记独立确定的脆性X染色体的存在之间存在对应关系。在124例中,正常1.0 kb PstI片段的存在与通过连锁侧翼标记独立确定的脆性X染色体的缺失之间也存在对应关系。另外六个被认为是“脆性X”孤立病例的家庭在FRAXD被识别之前就已被诊断。pfxa3探针在三个家庭中证实了细胞遗传学诊断,另外三个家庭被重新诊断为非脆性X。另外两个家庭有一个不同的叶酸敏感脆性位点FRAXE的一致表达,该位点靠近FRAXA,但与脆性X综合征无关,且不能被pfxa3探针检测到。随后从其他家庭成员或新家庭的成员那里收到了转诊,这些家庭成员的携带者状态尚未通过连锁标记预先确定。通过用对照探针pS8进行剂量分析,证实了这222例额外病例中135名女性的直接pfxa3诊断。(摘要截短于250字)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6ff/1015984/b9d052a39cb9/jmedgene00020-0011-a.jpg

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