Klinefelter's syndrome laboratory findings: Difference between revisions
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A [[karyotype]] is used to confirm the diagnosis. In this procedure, a small blood sample is drawn. [[White blood cell]]s are then separated from the sample, mixed with [[Growth medium|tissue culture medium]], incubated, and checked for chromosomal abnormalities, such as an extra X chromosome. | A [[karyotype]] is used to confirm the diagnosis. In this procedure, a small blood sample is drawn. [[White blood cell]]s are then separated from the sample, mixed with [[Growth medium|tissue culture medium]], incubated, and checked for chromosomal abnormalities, such as an extra X chromosome. | ||
[[Image:Human chromosomesXXY01.png|350px|thumb|center|Klinefelter's syndrome karyotype]] | |||
The following tests may be performed: | The following tests may be performed: |
Revision as of 15:55, 14 August 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Laboratory Findings
A karyotype is used to confirm the diagnosis. In this procedure, a small blood sample is drawn. White blood cells are then separated from the sample, mixed with tissue culture medium, incubated, and checked for chromosomal abnormalities, such as an extra X chromosome.

The following tests may be performed:
- Semen count
- Serum estradiol levels (a type of estrogen)
- Serum follicle stimulating hormone
- Serum luteinizing hormone
- Serum testosterone