Indications for the Test
- Diagnosing causes of male infertility
- Evaluating cases of small testicular size
- Investigating causes of low testosterone levels
- Genetic confirmation of Klinefelter Syndrome
Book Klinefelter Syndrome Genetic Test | Lahalak Medical Platform
This precise chromosomal analysis identifies genetic causes of infertility and low testosterone, enabling a comprehensive treatment plan to support your sexual and physical health effectively.
Scientific name: Karyotyping for Klinefelter Syndrome (47,XXY)
An advanced laboratory test analyzing chromosomes to detect Klinefelter Syndrome (47,XXY). It is essential for diagnosing male infertility and primary testicular failure to determine appropriate hormonal therapy.
Service type
Laboratory test
Duration
10-15 minutes
Fasting
Fasting is not required
Included Services
- Blood sample collection
- Chromosomal analysis
- Detailed medical report
Medical Service Information
Symptoms Requiring Analysis
- Difficulty conceiving despite attempts
- Low libido or erectile dysfunction
- Gynecomastia (enlarged male breast tissue)
- Abnormal height increase with muscle weakness
Understanding the Results
- Normal Result (46,XY): No chromosomal abnormalities detected
- Positive Result (47,XXY): Confirms Klinefelter Syndrome diagnosis
- Early diagnosis aids in starting hormone replacement therapy
Conditions & Notices
- No special preparation required before the test
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