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Chromosome 10p duplication syndrome: 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. More detailed information about the symptoms, causes, and treatments of Chromosome 10p duplication syndrome is available below.
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Duplication of the short arm of chromosome 10 with a variable phenotype depending on the size of the trisomic segment. Growth and mental retardation, craniofacial dysmorphism, and ocular, cardiovascular, skeletal, and other abnormalities are associated. - (Source - Diseases Database)
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