vitalwiki

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