48,XXYY синдром
ORPHA:10· ICD-10 Q98.8· 48,XXYY syndrome
Визначення(English summary)
A rare sex chromosome number anomaly disorder characterized, genetically, by the presence of an extra X and Y chromosome in males and, clinically, by tall stature, dysfunctional testes associated with infertility and insufficient testosterone production, cognitive, affective and social functioning impairments, global developmental delay, and an increased risk of congenital malformations.
- Поширеність
- Unknown
- Успадкування
- Not applicable, Unknown
- Вік початку
- Adolescent, Childhood, Infancy, Neonatal