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Klinefelter syndrome, variants

Klinefelter syndrome, variants: Introduction

Klinefelter syndrome, variants: A genetic condition where males have at least one extra X chromosome or extra copies of both the X and Y chromosomes in each cell. Normally male cells contain one X and one Y chromosome in each cell. The condition is not inherited but is a result of problems during cell division. More detailed information about the symptoms, causes, and treatments of Klinefelter syndrome, variants is available below.

Symptoms of Klinefelter syndrome, variants

Home Diagnostic Testing

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Wrongly Diagnosed with Klinefelter syndrome, variants?

Klinefelter syndrome, variants: Related Patient Stories

Klinefelter syndrome, variants: Complications

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Causes of Klinefelter syndrome, variants

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Disease Topics Related To Klinefelter syndrome, variants

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Less Common Symptoms of Klinefelter syndrome, variants

Klinefelter syndrome, variants: Undiagnosed Conditions

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Hospitals & Clinics: Klinefelter syndrome, variants

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Statistics for Klinefelter syndrome, variants

Klinefelter syndrome, variants: Broader Related Topics

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Definitions of Klinefelter syndrome, variants:

Klinefelter syndrome, variants is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Klinefelter syndrome, variants, or a subtype of Klinefelter syndrome, variants, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

 

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