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Distal duplication 18q syndrome

ORPHA:1716· ICD-10 Q92.3

Definition

A rare, partial autosomal trisomy characterized by a variable phenotype that includes hypotonia, motor delay, mild to severe intellectual disability, seizures, variable cerebral anomalies, finger/toe syndactyly, fifth finger clinodactyly, strabismus, short neck and dysmorphic facial features.

Prevalence
1-9 / 1 000 000
Age of onset
Antenatal, Neonatal