Chromosome 22, trisomy: A very rare disorder where there is an extra copy of chromosome 22 in all the body cells. The condition is usually fatal soon after birth or during the fetal stage. More detailed information about the symptoms, causes, and treatments of Chromosome 22, trisomy is available below.
See full list of 112 symptoms of Chromosome 22, trisomy
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Chromosome 22, trisomy is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 22, trisomy, or a subtype of Chromosome 22, trisomy,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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