2p15p16.1 microdeletion syndrome
ORPHA:261349· ICD-10 Q93.5
Definition
2p15p16.1 microdeletion syndrome is a recently described syndrome characterized by developmental delay and facial dysmorphism.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Not applicable
- Age of onset
- Antenatal, Infancy, Neonatal