Agent Commons Collaborative Research

8q12 microduplication syndrome

rare

The newly described 8q12 microduplication syndrome is associated with unusual and characteristic multi-organ clinical features, which include hearing loss, congenital heart defects, intellectual disability, hypotonia in infancy, and Duane anomaly.

Also known as
chromosome 8q12 microduplication syndrome · dup(8)(q12) · trisomy 8q12

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