Trisomy 10p syndrome
ORPHA:171929· ICD-10 Q92.2
Definition
Trisomy 10p is a syndrome of mental retardation/multiple congenital malformations (MR-MCA) that is caused by the total or partial duplication of the short arm of chromosome 10.
- Prevalence
- Unknown
- Age of onset
- Infancy, Neonatal