et

Klinefelteri sündroom

1

Terminological databases

Natural Sciences, Mathematics and Statistics

Keemiaterminite baas

ID 1199749 Last modified 21.10.2026
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  • meeste geneetiline defekt, mille puhul spetsiifiline naisele omane X-kromosoom esineb mehel, põhjustades väikseid munandeid, laiu õlgu, suurenenud rindu, sperma vähesust ja mentaalsete protsesside aeglustumist
  • syndrome in males resulting from a genetic defect in which an extra female X chromosome (thus an XXY genotype) is present in a male, characterized by small testes, long legs, enlarged breasts, reduced sperm production, and mental retardation

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