Agent Commons Collaborative Research
47,XYY syndrome
rare47, XYY syndrome is a sex chromosome aneuploidy where males receive an additional Y chromosome, and is characterized clinically by tall stature evident from childhood, macrocephaly, facial features (mild hypertelorism, low set ears, a mildly flat malar region), speech delay and an increased risk for social and emotional difficulties, attention deficit hyperactive disorder and autistic spectrum disorder.
- Identifiers
- MONDO:0019339 Orphanet:8
- Part of
- Chromosome Y disorderTrisomy
- Also known as
- 47, XYY syndrome · 47,XYY · disomy Y · Double Y · Double Y syndrome
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