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Up to: Partial duplication of the short arm of chromosome 17
Trisomy 17p
Trisomy 17p is a rare chromosomal abnormality resulting from the duplication of the short arm of chromosome 17 and characterized by pre- and post-natal growth retardation, developmental delay, hypotonia, digital abnormalities, congenital heart defects, and distinctive facial features.
This condition has no sub-types.