Синдром проксимальної делеції 4q25
ORPHA:502437· ICD-10 Q93.5· 4q25 proximal deletion syndrome
Визначення(English summary)
A partial deletion of the long arm of chromosome 4 characterized by complex behavioral difficulties, developmental and delay/ intellectual disability, and minor dysmorphic features, including subtle facial asymmetry (most prominent in the mandible), mild hypotelorism, long nasal bridge, small low-set ears, narrow mouth, and mild hand deformities, such as bilateral short 5th metacarpals, and short hands.
- Поширеність
- <1 / 1 000 000
- Вік початку
- Infancy