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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
(14)
Chromosomal disorder
(12)
Disease of genetic or genomic mechanism
(2)
Autosomal anomaly
(0)
Chromosome 17 disorder
(0)
Disease by etiologic mechanism
(0)
Partial duplication of chromosome 17
(0)
Partial duplication of the short arm of chromosome 17
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Syndrome caused by partial chromosomal duplication
(0)