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Mosaicism and uniparental disomy in prenatal diagnosis

Journal

TRENDS IN MOLECULAR MEDICINE
Volume 21, Issue 2, Pages 77-87

Publisher

CELL PRESS
DOI: 10.1016/j.molmed.2014.11.010

Keywords

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Funding

  1. Bundesministerium fur Bildung und Forschung (Network 'Imprinting Diseases') [01GM1114C, 01GM114B]

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Chromosomal mosaicism is the presence of numerous cell lines with different chromosomal complements in the same individual. Uniparental disomy (UPD) is the inheritance of two homologous chromosomes from the same parent. These genetic anomalies arise from errors in meiosis and/or mitosis and can occur independently or in combination. Due to the formation mechanisms of UPD, low-level or undetected mosaicisms are assumed for a significant number of UPD cases. The pre- and postnatal clinical consequences of mosaicism for chromosomal aberrations and/or UPD depend on the gene content of the involved chromosome. In prenatal evaluation of chromosomal mosaicism and UPD, genetic counseling should be offered before any laboratory testing.

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