An incidental finding of maternal multiple myeloma by non invasive prenatal testing

Non invasive prenatal testing for fetal trisomies 13, 18, and 21 occasionally identifies maternal cancer. A further case of maternal cancer incidentally diagnosed by routine NIPT. Extensive NIPT abnormalities are unlikely to be of fetal origin. Information given to patients should also adequately ad...

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Detalles Bibliográficos
Autores principales: Imbert‐Bouteille, Marion, Chiesa, Jean, Gaillard, Jean‐Baptiste, Dorvaux, Véronique, Altounian, Lucille, Gatinois, Vincent, Mousty, Eve, Finge, Sanae, Bourquard, Pascal, Vermeesch, Joris Robert, Legius, Eric, Vandenberghe, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Research Letters
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767741/
https://www.ncbi.nlm.nih.gov/pubmed/29023902
http://dx.doi.org/10.1002/pd.5168
Descripción
Sumario:Non invasive prenatal testing for fetal trisomies 13, 18, and 21 occasionally identifies maternal cancer. A further case of maternal cancer incidentally diagnosed by routine NIPT. Extensive NIPT abnormalities are unlikely to be of fetal origin. Information given to patients should also adequately advise patients on potential incidental findings and might offer the option to opt out of receiving results beyond the trisomy report. International guidelines would improve patient counseling.

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