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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