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Analysis of Sex Chromosomes in Preimplantation Genetic Diagnosis for X-Chromosome-Linked Disorders

机译:X染色体相关疾病的植入前遗传学诊断中性染色体的分析

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摘要

Preimplantation genetic diagnosis (PGD) is diagnostic tool to avoid inheritance of genetic disease by transferring unaffected embryos. Recently, PCR and FISH have been mainly applied to the diagnosis of single gene disorders and chromosomal abnormalities, respectively. Since with PGD, only a few cells are available for genetic tests, both gene and chromosomes analysis have to be obtained from the same, limited material. Cell recycling makes it possible to obtain the information on genes as well as chromosomes from the same cells. Therefore cell recycling is an acceptable strategy where in PGD targets large proportions of embryos severe chromosomal abnormalities. The responsible genes of the X-linked disorder and numerical abnormalities of sex chromosomes should be analyzed simultaneously. Gender information is definitely useful because only male affected embryos should be avoided for transfer.
机译:植入前遗传学诊断(PGD)是通过转移未受影响的胚胎来避免遗传疾病遗传的诊断工具。近来,PCR和FISH分别主要用于单基因疾病和染色体异常的诊断。由于使用PGD,只有少数细胞可用于基因测试,因此必须从相同的有限材料中进行基因和染色体分析。细胞回收使从同一细胞获得有关基因和染色体的信息成为可能。因此,细胞回收是一种可接受的策略,其中PGD以大比例的胚胎为目标,导致严重的染色体异常。应当同时分析X连锁疾病的负责基因和性染色体的数字异常。性别信息绝对有用,因为只有男性受影响的胚胎才应避免转移。

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