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Placental mosaicism in the era of chromosomal microarrays.
Vogel, Ida; Vestergaard, Else Marie; Lildballe, Dorte Launtoft; Christensen, Rikke; Hoseth, Gerd-Eva; Petersen, Astrid Christine; Bogaard, Pauline; Sørensen, Anne Nødgaard.
Afiliación
  • Vogel I; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark. Electronic address: idavogel@rm.dk.
  • Vestergaard EM; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Biochemistry, Horsens Regional Hospital, Horsens, Denmark.
  • Lildballe DL; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Genetics, Vejle Hospital, Aarhus, Denmark.
  • Christensen R; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark.
  • Hoseth GE; Department of Gynecology and Obstetrics, Aalborg University Hospital, Denmark.
  • Petersen AC; Department of Pathology, Aalborg University Hospital, Denmark.
  • Bogaard P; Department of Pathology, Aalborg University Hospital, Denmark.
  • Sørensen AN; Department of Gynecology and Obstetrics, Aalborg University Hospital, Denmark; Department of Clinical Medicine, Aalborg University Hospital, Aalborg University, Denmark.
Eur J Med Genet ; 63(4): 103778, 2020 Apr.
Article en En | MEDLINE | ID: mdl-31580923
OBJECTIVE: Placental mosaicism for a subset of a chromosome, a structural chromosomal aberration, is thought to be a very rare finding in chorionic villus samples. Here, we present clinical and laboratory data on five cases with such mosaicism for structural chromosomal aberrations. METHODS: During a period of 6 months, chromosomal microarray was carried out on DNA extracted from 100 uncultured chorion villous samples from high-risk pregnancies. RESULTS: In five of 100 consecutively collected samples (5/100), mosaicism for a structural chromosomal aberration was detected. The mosaic aberration was subsequently detected in fetal tissue in three of the five cases. CONCLUSION: Chromosomal microarray can detect placental mosaicism for structural chromosomal aberrations. This kind of mosaicism may be more frequent than previously anticipated, and the fetal involvement seems difficult to predict. These findings highlight the complexity of mosaicism for structural chromosomal aberrations in prenatal samples in the chromosomal microarray era.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Placenta / Muestra de la Vellosidad Coriónica / Trastornos de los Cromosomas / Amniocentesis / Mosaicismo Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Middle aged / Pregnancy Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Placenta / Muestra de la Vellosidad Coriónica / Trastornos de los Cromosomas / Amniocentesis / Mosaicismo Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Middle aged / Pregnancy Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article Pais de publicación: Países Bajos