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Chromosome 17 ring: A rare chromosomal disorder where genetic material from one or both ends of chromosome 17 is missing and the two broken ends have rejoined to form a ring. The resulting type and severity of symptoms is determined by the amount and location of genetic material missing. More detailed information about the symptoms, causes, and treatments of Chromosome 17 ring is available below.
Read more about causes of Chromosome 17 ring.
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Chromosome 17 ring 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 ring, or a subtype of Chromosome 17 ring,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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