Трисомія 18
ORPHA:3380· ICD-10 Q91.0· Trisomy 18 syndrome
Визначення(English summary)
Trisomy 18 is a chromosomal abnormality associated with the presence of an extra chromosome 18 and characterized by growth delay, dolichocephaly, a characteristic facies, limb anomalies and visceral malformations.
- Поширеність
- 1-5 / 10 000
- Успадкування
- Not applicable, Unknown
- Вік початку
- Antenatal, Neonatal