Duplication 10p (medical condition): A rare chromosomal disorder where there are three copies of the short arm (p) of chromosome 10 rather than the normal two resulting in various abnormalities. The type and severity of symptoms depend on the amount and location of genetic material duplicated.
See also:
Duplication 10p:
»Introduction: Duplication 10p
»Symptoms of Duplication 10p
»Treatments for Duplication 10p
These medical condition or symptom topics may be relevant to medical information for Duplication 10p:
Duplication 10p is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Duplication 10p, or a subtype of Duplication 10p,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Duplication 10p as a "rare disease".
Source - Orphanet
Duplication 10p (medical condition): See Duplication 10p (disease information).
»Introduction: Duplication 10p
»Symptoms of Duplication 10p
»Treatments for Duplication 10p
Source - NIH
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