Синдромна Х-зчеплена інтелектуальна недостатність, повязана з KDM5C
ORPHA:85279· ICD-10 Q87.8· KDM5C-related syndromic X-linked intellectual disability
Визначення(English summary)
A rare multiple congenital anomalies/dysmorphic syndrome characterized by mild to severe intellectual deficit associated with variable clinical manifestations including spasticity, cryptorchidism, maxillary hypoplasia, alopecia areata, epilepsy, short stature, impaired speech, and behavioral problems.
- Поширеність
- <1 / 1 000 000
- Успадкування
- X-linked recessive
- Вік початку
- Childhood