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Showing 1 to 3 of 3 for “"Klinefelter's syndrome"”.

  1. 'A common condition: a rare diagnosis?' What is the significance of diagnosis in Klinefelter’s Syndrome (47, xxy)?

    Klinefelter's Syndrome (47,XXY) is a sporadic, non-inherited genetic condition occurring only in males where there is the presence of an additional X chromosome. Although not well known, Klinefelter's Syndrome is reported to be relatively common with an estimated incidence of between approximately …

    bournemouth Repository record for 'A common condition: a rare diagnosis?' What is the significance of diagnosis in Klinefelter’s Syndrome (47, xxy)? (opens in a new tab)

  2. Karyotypes and Case Studies of Ten Individuals With Suspected Sex Chromosome Anomalies

    … Two male residents suspected of having Turner's syndrome in the male were found to have a 46,XY chromosome complement. One male resident with a Klinefelter's phenotype had a 46,XY chromosome complement. One male had a 49,XXXXY chromosome complement. Conclusions. The six females in the study were …

    drake Repository record for Karyotypes and Case Studies of Ten Individuals With Suspected Sex Chromosome Anomalies (opens in a new tab)

  3. An Exploratory Study of Physical Phenotype, Biomarkers and Psychosocial Health Parameters in Boys with Klinefelter Syndrome

    Klinefelter Syndrome (KS) is a genetic condition that occurs only in males. In adult men, KS is associated with reproductive, cardiometabolic, bone and psychosocial health problems that are believed to emerge during peri-puberty. In children, the condition is under-diagnosed and not well understood …

    columbia-diss Repository record for An Exploratory Study of Physical Phenotype, Biomarkers and Psychosocial Health Parameters in Boys with Klinefelter Syndrome (opens in a new tab)