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10q Partial Trisomy: A very rare genetic disorder characterized by the duplication of genetic material from the long arm (q) of chromosome 10 - the genetic material occurs three times in body cells instead of the normal two. The type and severity of symptoms may vary considerably depending on the exact location and size of the duplicated genetic material. More detailed information about the symptoms, causes, and treatments of 10q Partial Trisomy is available below.
See full list of 14 symptoms of 10q Partial Trisomy
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Prognosis for 10q Partial Trisomy: The prognosis varies depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.
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Types of 10q Partial Trisomy
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10q Partial Trisomy is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that 10q Partial Trisomy, or a subtype of 10q Partial Trisomy,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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