Синдром мікроделеції 20p12.3
ORPHA:261295· ICD-10 Q93.5· 20p12.3 microdeletion syndrome
Визначення(English summary)
20p12.3 microdeletion syndrome is a recently described syndrome characterized by Wolff-Parkinson-White syndrome (see this term), variable developmental delay and facial dysmorphism.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Not applicable, Unknown
- Вік початку
- Infancy, Neonatal