Синдром мікроделеції 6p22
ORPHA:251046· ICD-10 Q93.5· 6p22 microdeletion syndrome
Визначення(English summary)
6p22 microdeletion syndrome is a newly described syndrome associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Not applicable, Unknown
- Вік початку
- Infancy, Neonatal