1p21.3 microdeletion syndrome
ORPHA:293948· ICD-10 Q93.5
Definition
1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterized by severe speech and language delay, intellectual deficiency, autism spectrum disorder.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Unknown
- Age of onset
- No data available