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There were total 24 embryos transplanted in 14 embryo transfer cycles (1.47 ± 0.75 embryos per transfer). There were 12 biochemical pregnancies obtained (85.71% per transfer cycle), 14 embryos implanted (58.33% per transferred embryo), and there were 11 clinical pregnancies with births of 3 healthy boys and 8 healthy girls and 3 ongoing clinical pregnancies (78.57% per transfer cycle). And, no patient underwent prenatal diagnosis which was recommended strongly or karyotype detection of newborns. There are 90 embryos with two sex chromosomal signals among 103 embryos with clear diagnosis (87.38%), and the number of those with XX is 49, slightly more than those with XY (41). 13 abnormal embryos are with one, three, or four sex chromosomal signals (3 with X, 1 with XYY, 3 with XXY, 4 with XXX, and 2 with XXYY). In 2003, Staessen et al. demonstrated their embryonic detection outcomes with Fluorescence In Situ Hybridization (FISH) that the proportion of normal embryos (54%) is significantly lower than controls (77.2%), who are with X-linked disease in need of PGD to determine gender. Among the abnormal embryos, the rate of sex chromosomal abnormalities is 13.2%, much higher than controls (3.1%). The other study in 2003 found that in embryos detected for chromosomes 13, 18, 21, X and Y, 14 out of 23 embryos were diagnosed as normal (60.9%), and 5 in 28 (17.8%) were diagnosed as abnormal with sex chromosomal abnormalities.2 In our study, embryos were analyzed only for sex chromosomes, and the proportion of abnormal embryos is 12.62% (13 in 103). And, there is no statistically significant difference between our outcomes and those we have mentioned1,2 (Chi-square test, in Table 1). Considering one patient is mosaic, the proportion of abnormal embryos is 12.62% if we take him into consideration (13 in 103); while it is 11.76% if we exclude him (10 in 85). There is also no statistically significant difference compared with the historical data (Chi-square test: P = 0.752, P = 0.615, respectively). As both historical studies above were almost those with TESE, the comparison result also implies that the proportion of abnormal embryos from ejaculated spermatozoa is comparable with those from TESE, at least for sex chromosomes. In addition, excluding the couple in our study beyond 35 years old, the proportion of abnormal embryos is 11.76% (10 out of 85), much higher than the embryonic aneuploidy rate of sex chromosomes (3.4%, 235 out of 6819) in the population with infertility under 35 as mentioned.3 In spite of the higher aneuploidy rate of embryos in KS patients, there are at least 200 normal babies born with ICSI without PGD Dear Editor, Klinefelter syndrome (KS) is the most frequent genetic cause of infertility in men. Paternity can be achieved through intracytoplasmic sperm injection (ICSI) with spermatozoa recovered from ejaculated semen if exist, or testes with testicular sperm extraction (TESE). Though the proportion of spermatozoa and embryos with abnormal sex chromosomes and autosomes, especially chromosomes 13,18 and 21, is higher in KS patients as reported,1 which suggests the need of preimplantation genetic diagnosis (PGD), the application of PGD becomes questionable with more and more normal babies born with ICSI without PGD. This article aims to report the results of 13 ICSI-PGD cycles performed in 13 KS patients with ejaculated spermatozoa in the authors’ reproductive center and to discuss the necessity of application of PGD in comparison with the outcomes of ICSI with or without PGD in KS patients in literature (P < 0.05 was considered to be statistically significant). The mean (±s.d.) age of 13 male partners is 28.62 ± 5.33 (maximum age 44 years), while the mean (±s.d.) age of female partners is 27.94 ± 5.37 (maximum age 43 years). Twelve patients were karyotyped with 47, XXY; the other one was mosaic with 47, XXY[74]/46, XY[26]. They all were characterized with micropenis and small atrophic testes, along with elevated Follicle-Stimulating Hormone (FSH) and Luteiniz ing Hormone (LH) (FSH 30.00 ± 14.29 IU·L-1, LH 15.92 ± 5.80 IU·L−1) and lower or relatively normal testosterone (251.77 ± 157.40 ng·dl−1). Three of them had unapparent prominentia laryngea and sparse pubic hair, while other ones were normal. All patients presented oligoasthenozoospermia, from slight to severe. As semen analysis on the day of oocyte retrieval showed, only one or two spermatozoa with low motility can be found in each high power field in six of them. Another one was evaluated with the presence of sperm cells after high-speed centrifugation (1800 g). Sperm concentration of the others was from 1 to 7 million·ml−1 and the sperm motility was from 3% to 15%. LETTER TO THE EDITOR

Outcomes of 13 ICSI-PGD cycles with ejaculated spermatozoa in patients with Klinefelter syndrome