A case of a rare variant of Klinefelter syndrome, 47,XY,i(X)(q10) |
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| Authors: | T. Kondo S. Kuroda K. Usui K. Mori T. Asai T. Takeshima T. Kawahara H. Hamanoue H. Uemura Y. Yumura |
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| Affiliation: | 1. Department of Urology, Reproduction Center, Yokohama City University Medical Center, Yokohama, Japan;2. Department of Urology and Renal Transplantation, Yokohama City University Medical Center, Yokohama, Japan;3. Department of Clinical Genetics, Yokohama City University Hospital, Yokohama, Japan |
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| Abstract: | Klinefelter syndrome is a condition in which a male patient has one Y chromosome and one or more extra X chromosomes. It is the most common sex chromosome disorder. Klinefelter syndrome is distinguished by many clinical features, such as infertility, high gonadotropin and low testosterone levels, increased height, and sparse body and facial hair. We report the case of a 32‐year‐old man who visited our hospital complaining of male infertility. Semen analysis showed azoospermia, and chromosomal analysis revealed a 47,XY,i(X)(q10) karyotype, which is a rare variant of Klinefelter syndrome. No spermatozoon was found on microdissection testicular sperm extraction, and the testis biopsy histology showed only Sertoli cells and hyalinised seminiferous tubules. 47,XY, i(X)(q10) has an additional isochromosome made of the long arm of the X chromosome, which shares some features of classical Klinefelter syndrome in many aspects, but patients are usually shorter than average height and have normal intelligence. In addition, to the best of our knowledge, no successful sperm extractions from 47,XY, i(X)(q10) patients were reported in the literature. The reports of patients who have undergone microdissection testicular sperm extraction are very rare. Further reports and studies of this chromosomal abnormality are needed. |
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| Keywords: | azoospermia isochromosome Klinefelter syndrome |
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