Detection of a case of chronic myeloid leukaemia with deletions at the t(9;22) translocation breakpoints by a genome‐wide non‐invasive prenatal test
What's Already Known about this Topic? Incidental findings occur when undergoing a non‐invasive prenatal test (NIPT). Incidental findings are not necessarily fetal in origin but can be maternal as well. Aberrant NIPT patterns can be indicative of a maternal cancer, but only very few reports have been published thus far. What does this Study Add? This study is the first to report that genome‐wide NIPT can detect chronic myeloid leukaemia caused by the typical t(9;22) translocation when accompanied by deletions at the translocation breakpoints..
Medienart: |
Artikel |
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Erscheinungsjahr: |
2016 |
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Erschienen: |
2016 |
Enthalten in: |
Zur Gesamtaufnahme - volume:36 |
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Enthalten in: |
Prenatal diagnosis - 36(2016), 8, Seite 760-765 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Janssens, Katrien [VerfasserIn] |
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doi: |
10.1002/pd.4857 |
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funding: |
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PPN (Katalog-ID): |
OLC1980258988 |
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245 | 1 | 0 | |a Detection of a case of chronic myeloid leukaemia with deletions at the t(9;22) translocation breakpoints by a genome‐wide non‐invasive prenatal test |
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520 | |a What's Already Known about this Topic? Incidental findings occur when undergoing a non‐invasive prenatal test (NIPT). Incidental findings are not necessarily fetal in origin but can be maternal as well. Aberrant NIPT patterns can be indicative of a maternal cancer, but only very few reports have been published thus far. What does this Study Add? This study is the first to report that genome‐wide NIPT can detect chronic myeloid leukaemia caused by the typical t(9;22) translocation when accompanied by deletions at the translocation breakpoints. | ||
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700 | 1 | |a Beckers, Sigri |4 oth | |
700 | 1 | |a Holmgren, Philip |4 oth | |
700 | 1 | |a Vermeulen, Katrien |4 oth | |
700 | 1 | |a Maes, Marie‐Berthe |4 oth | |
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