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Дистальна делеція 12p

ORPHA:280325· ICD-10 Q93.5· Distal deletion 12p syndrome

Визначення(English summary)

A rare partial autosomal monosomy characterized by language development delay with childhood apraxia of speech, mild intellectual disability, behavourial abnormalities (autistic spectrum disorder, attention deficit hyperactivity disorder, anxiety) and mildly dysmorphic nonspecific features. Additional clinical features may include muscular hypotonia and joint laxity, hernias and microcephaly.

Поширеність
<1 / 1 000 000
Вік початку
Infancy, Neonatal