Синдром мікроделеції 1q41q42
ORPHA:250999· ICD-10 Q93.5· 1q41q42 microdeletion syndrome
Визначення(English summary)
1q41q42 microdeletion syndrome is a chromosomal anomaly characterized by a severe developmental delay and/or intellectual disability, typical facial dysmorphic features, brain anomalies, seizures, cleft palate, clubfeet, nail hypoplasia and congenital heart disease.
- Поширеність
- Unknown
- Успадкування
- Not applicable, Unknown
- Вік початку
- Infancy, Neonatal