Chromosome 17, trisomy 17p11.2: A rare chromosomal disorder where a portion of the short arm of chromosome 17 is duplicated. More detailed information about the symptoms, causes, and treatments of Chromosome 17, trisomy 17p11.2 is available below.
See full list of 14 symptoms of Chromosome 17, trisomy 17p11.2
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Chromosome 17, trisomy 17p11.2 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 17, trisomy 17p11.2, or a subtype of Chromosome 17, trisomy 17p11.2,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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