Health / Medical Topics |
Trisomy 13
A chromosomal abnormality characterized by the presence of three copies of genetic material for chromosome 13, instead of the normal two. It leads to a variety of abnormalities that include mental retardation, microcephaly, low-set ears, eye structural defects, polydactyly, and limb abnormalities. (NCI Thesaurus)
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A chromosomal abnormality consisting of the presence of a third copy of chromosome 12 in somatic cells.
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