Cargando…

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...

Descripción completa

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

Ejemplares similares

Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variations
por: Gatinois, Vincent, et al.
Publicado: (2019)

Noninvasive prenatal testing detected acute myeloid leukemia in paucisymptomatic pregnant patient
por: Rengifo, Laura Yissel, et al.
Publicado: (2020)

Somatic Genomic Variations in Early Human Prenatal Development
por: Robberecht, Caroline, et al.
Publicado: (2010)

Pregnant women with confirmed neoplasms should not have noninvasive prenatal testing
por: Lenaerts, Liesbeth, et al.
Publicado: (2019)

AnnotSV and knotAnnotSV: a web server for human structural variations annotations, ranking and analysis
por: Geoffroy, Véronique, et al.
Publicado: (2021)

Pathogenesis of vestibular schwannoma in ring chromosome 22
por: Denayer, Ellen, et al.
Publicado: (2009)

Piecing together the problems in diagnosing low-level chromosomal mosaicism
por: Robberecht, Caroline, et al.
Publicado: (2010)

Assessment of All-Cause Cancer Incidence Among Individuals With Preeclampsia or Eclampsia During First Pregnancy
por: Serrand, Chris, et al.
Publicado: (2021)

Incidental Prenatal Diagnosis of Sex Chromosome Aneuploidies: Health, Behavior, and Fertility
por: Pieters, J. J. P. M., et al.
Publicado: (2011)

Prenatal Diagnosis of Cystic Fibrosis and Hemophilia: Incidental Findings and Weak Points
por: Comegna, Marika, et al.
Publicado: (2019)

Fetal sex determination in twin pregnancies using non-invasive prenatal testing
por: Villela, Darine, et al.
Publicado: (2019)

Incidental Discovery of a Testicular Plasmacytoma at Initial Presentation of Multiple Myeloma
por: Hathaway, Amanda R.
Publicado: (2013)

Incidental multiple myeloma in a patient with neuroretinitis: a case report
por: Joo, Taesung, et al.
Publicado: (2023)

A framework for reporting secondary and incidental findings in prenatal sequencing: When and for whom?
por: Vears, Danya, et al.
Publicado: (2022)

Obstetric antiphospholipid syndrome: early variations of angiogenic factors are associated with adverse outcomes
por: Cochery-Nouvellon, Éva, et al.
Publicado: (2017)

Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis
por: Westerfield, Lauren, et al.
Publicado: (2014)

Cat Dilemma: Too Protected To Escape Trophy Hunting?
por: Palazy, Lucille, et al.
Publicado: (2011)

Chromosomal phenotypes and submicroscopic abnormalities
por: Devriendt, Koen, et al.
Publicado: (2004)

The 22q11.2 Low Copy Repeats
por: Vervoort, Lisanne, et al.
Publicado: (2022)

Disruption of chromatin organisation causes MEF2C gene overexpression in intellectual disability: a case report
por: Yauy, Kevin, et al.
Publicado: (2019)

Unexpected discovery of multiple myeloma following cardiomyopathy
por: Dahraoui, Souhail, et al.
Publicado: (2017)

baredSC: Bayesian approach to retrieve expression distribution of single-cell data
por: Lopez-Delisle, Lucille, et al.
Publicado: (2022)

Prenatal Detection of Uniparental Disomies (UPD): Intended and Incidental Finding in the Era of Next Generation Genomics
por: Eggermann, Thomas
Publicado: (2020)

Increased incidence of cancer in the follow-up of obstetric antiphospholipid syndrome within the NOH-APS cohort
por: Gris, Jean-Christophe, et al.
Publicado: (2020)

Impact of systematic urinary catheterization protocol in delivery room on covert postpartum urinary retention: a before-after study
por: Neron, Mathias, et al.
Publicado: (2017)

Vital NETosis vs. suicidal NETosis during normal pregnancy and preeclampsia
por: Guillotin, Florence, et al.
Publicado: (2023)

Incidental finding of maternal malignancy in an unusual non‐invasive prenatal test and a review of similar cases
por: Moellgaard, Maria Hammer, et al.
Publicado: (2022)

Confined Growth of NiAl-Layered Double Hydroxide Nanoparticles Within Alginate Gel: Influence on Electrochemical Properties
por: Prevot, Vanessa, et al.
Publicado: (2020)

Chromoanagenesis: a piece of the macroevolution scenario
por: Pellestor, Franck, et al.
Publicado: (2020)

Osteolytic Lesion of the Maxilla in an Undiagnosed Multiple Myeloma Patient Identified Incidentally by Cone Beam Computed Tomography
por: Ali, Sarah AlFarabi, et al.
Publicado: (2022)

Prenatal ultrasound diagnosis of cystic biliary atresia
por: Morel, Baptiste, et al.
Publicado: (2015)

First Case Report of Maternal Mosaic Tetrasomy 9p Incidentally Detected on Non-Invasive Prenatal Testing
por: Shu, Wendy, et al.
Publicado: (2021)

Incidental Detection of a Chromosomal Aberration by Array-CGH in an Early Prenatal Diagnosis for Monogenic Disease on Coelomic Fluid
por: Vinciguerra, Margherita, et al.
Publicado: (2022)

Giardia lamblia Diagnosed Incidentally by Duodenal Biopsy
por: Groudan, Kevin, et al.
Publicado: (2021)

Comprehensive genome-wide analysis of routine non-invasive test data allows cancer prediction: A single-center retrospective analysis of over 85,000 pregnancies
por: Lenaerts, Liesbeth, et al.
Publicado: (2021)

Incidental Discovery of Multiorgan Extramedullary Plasmacytomas in the Setting of Newly Diagnosed Multiple Myeloma and Delayed Hemolytic Transfusion Reaction
por: Cook, Joselle, et al.
Publicado: (2017)

Incidentes /
por: Barthes, Roland
Publicado: (1987)

Skeletal muscle repair by adult human mesenchymal stem cells from synovial membrane
por: De Bari, Cosimo, et al.
Publicado: (2003)

Meiotic errors followed by two parallel postzygotic trisomy rescue events are a frequent cause of constitutional segmental mosaicism
por: Robberecht, Caroline, et al.
Publicado: (2012)

Single Circulating Fetal Trophoblastic Cells Eligible for Non Invasive Prenatal Diagnosis: the Exception Rather than the Rule
por: Cayrefourcq, Laure, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_21abg59dilbk4bb6ubhtj05de0