Trisomy 17p
MONDO:0016840Trisomy 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.
Also known as: dup(17p), trisomy type 17p, 17p duplication, 17p trisomy, Duplication 17p, chromosome 17p duplication, partial trisomy 17p
3 clinical trials for this condition and its sub-types.
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Disease
(618)
Human disease
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Chromosomal disorder
(12)
Disease of genetic or genomic mechanism
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Autosomal anomaly
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Chromosome 17 disorder
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Disease by etiologic mechanism
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Partial duplication of chromosome 17
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Partial duplication of the short arm of chromosome 17
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Syndrome caused by partial chromosomal duplication
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