Синдром делеції 21q
ORPHA:574· ICD-10 Q93.0· 21q deletion syndrome
Визначення(English summary)
Monosomy 21 is a chromosomal anomaly characterized by the loss of variable portions of a segment of the long arm of chromosome 21 that leads to an increased risk of birth defects, developmental delay and intellectual deficit.
- Поширеність
- <1 / 1 000 000
- Вік початку
- Antenatal, Neonatal