Синдром мікроделеції 17q11
ORPHA:97685· ICD-10 Q85.0· 17q11 microdeletion syndrome
Визначення(English summary)
17q11 microdeletion syndrome is a rare severe form of neurofibromatosis type 1 (NF1; see this term) characterized by mild facial dysmorphism, developmental delay, intellectual disability, increased risk of malignancies, and a large number of neurofibromas.
- Поширеність
- Unknown
- Успадкування
- Not applicable
- Вік початку
- Antenatal, Infancy, Neonatal