xxy

Results: According to the patients ′ cytogenetics examination, it is found there are 11 cases abnormal chromosomal karyotypes, including 6 cases of chromosome translocation, 2 cases of 47, XXY, 3 cases of big Y chromosome.

结果发现异常核型11例，其中染色体易位6例、2例47，XXY、3例大Y染色体。

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Patients with Klinefelter's syndrome are generally characterized by a 47, XXY karyotype, seminiferous tubule dysgenesis, azoospermia and infertility.

Klinefelter综合征患者以47，XXY核型，睾丸精曲小管发育不良，无精子症和不育为特征。

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Incontinentia pigmenti in a boy with XXY mosaicism detected by fluorescence in situ hybridization

1例荧光原位杂交检测存在XXY镶嵌的男孩出现色素失禁症

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Then were big Y chromosome, four cases, accounting for 7.02% of patients studied and 17.39% of those with ACK: 46, XY/ 47, XXY and 47, XXY, one case for each type.

其次为大Y染色体4例，检出率为7.02%，占异常核型的7.39%。46，XY/47，XXY和47，XYY各1例，检出率为1.75%，占异常核型的4.35%。

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In rare cases, there are problematic exceptions, for example combinations like XXY or XYY or XXX.

在罕见的案例里, 有一些成问题的例外, 例如,像XXY或XYY或 XXX的染色体复合的构成.

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Objective: To observe the segregation of sex chromosomes in the spermatozoa of a 46, XY/ 47, XXY patient with oligozoospermia.

目的：观察1例46，XY/47，XXY少精子症患者精子性染色体分离的情况。

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Case of partial mole was triploid, 69, XXY and with a chromosomal contribution from the female gamete.

1例部分性葡萄胎为三倍体，69，XXY，来源为双精子与一卵子结合而成。文章对完全性葡萄胎和部分性葡萄胎的发生来源做了简要的讨论。

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