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Chromosome 3, Trisomy 3q2: A rare chromosomal disorder involving the duplication of a portion of the long arm of chromosome 3. The symptoms are determined by the size and exact location of the duplicated portion. More detailed information about the symptoms, causes, and treatments of Chromosome 3, Trisomy 3q2 is available below.
See full list of 18 symptoms of Chromosome 3, Trisomy 3q2
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Chromosome 3, Trisomy 3q2 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 3, Trisomy 3q2, or a subtype of Chromosome 3, Trisomy 3q2,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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