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Aug 29, 2022 · An unusually tall, wide-hipped man who died 1,000 years ago in Portugal was the oldest known carrier of Klinefelter syndrome, a rare genetic condition in which males are born with an extra copy...
Aug 30, 2022 · The earliest ever recorded case of the genetic condition Klinefelter Syndrome has just been discovered – in a 1,000-year-old skeleton excavated from an archeological site in Portugal.
On examination, we found the outstandingly well preserved skeleton of an adult who was likely to have been more than 25 years old at the time of death. The person was approximately 1·80 m tall.
Aug 30, 2022 · A multidisciplinary team of researchers have discovered what is believed to be the oldest case of Klinefelter syndrome in a 1,000-year-old skeleton. The finding is outlined in a new study published in T...
Aug 29, 2022 · The statuesque skeleton was one of a few dozen excavated from the mountainous medieval archaeological site of Torre Velha in north-eastern Portugal, between 2012 and 2015.
May 9, 2024 · This study presents a unique case of Klinefelter syndrome, a chromosomal disorder characterized by a typical karyotype of 47, XXY, accompanied by a rare mosaic form of 47, XXY, and 48, XXXY, associated w...
Sep 16, 2022 · Klinefelter Syndrome is a super rare genetic but non-hereditary condition that gives men an extra X chromosome (also called the “47,XXY” syndrome). The genetic condition was found in an...
Aug 28, 2022 · Klinefelter Syndrome is a super rare genetic but non-hereditary condition that gives men an extra X chromosome (also called the “47,XXY” syndrome). The genetic condition was found in an 11th-century ske...
Mar 29, 2024 · 47,XXY is not rare and occurs 1 in 500 male births, however only about 25% of boys with 47, XXY (KS) are diagnosed and this diagnosis usually occurs in adulthood (Gravholt et al., 2018).
Dec 4, 2024 · Less than 20 cases of association of 46, XX / 47, XXY and OT DSD have been reported in the literature. We report in this study a case of this association and a review of all the cases reported in the lit...
