Chromosome 10, trisomy 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:
Chromosome 10, trisomy 10p:
»Introduction: Chromosome 10, trisomy 10p
»Symptoms of Chromosome 10, trisomy 10p
»Treatments for Chromosome 10, trisomy 10p
These medical condition or symptom topics may be relevant to medical information for Chromosome 10, trisomy 10p:
Chromosome 10, trisomy 10p is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 10, trisomy 10p, or a subtype of Chromosome 10, trisomy 10p,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Chromosome 10, trisomy 10p (medical condition): See Chromosome 10, trisomy 10p (disease information).
»Introduction: Chromosome 10, trisomy 10p
»Symptoms of Chromosome 10, trisomy 10p
»Treatments for Chromosome 10, trisomy 10p
Source - NIH
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