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48,XXYY syndrome

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

The 48,XXYY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of an extra X and Y chromosome in males.

Synonyms

  • 48, XXYY Syndrome
  • 48, XXYY syndrome
  • 48,XXYY Klinefelter syndrome
  • 48,XXYY variant of Klinefelter's syndrome
  • XXYY syndrome48, XXYY Syndrome
  • 48, XXYY syndrome
  • 48,XXYY Klinefelter syndrome
  • 48,XXYY variant of Klinefelter's syndrome
  • XXYY syndrome
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