Monosomy

​Monosomy

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Monosomy refers to the condition in which only one chromosome from a pair is present in cells rather than the two copies usually found in diploid cells. When cells have one chromosome from a pair plus a portion of the second chromosome, this is referred to as partial monosomy. Monosomy, or partial monosomy, causes certain human diseases such as Turner syndrome and Cri du chat syndrome.

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Monosomy
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Monosomy. Formally, monosomy refers to the status of a cellular genome where one copy of a chromosome pair is absent. The term has also been expanded to situations where a segment of a chromosome, perhaps even just a single gene, is absent from a copy of a chromosome.

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Leslie G. Biesecker, M.D.
Leslie G. Biesecker, M.D.

Director & NIH Distinguished Investigator

Center For Precision Health Research

Autosome Genotype Mutation Birth Defect