Molecular cytogenetic analysis of term placentae suspected of mosaicism using fluorescence in situ hybridization. 1993

G H Schuring-Blom, and M Keijzer, and M E Jakobs, and D M Van den Brande, and H M Visser, and J Wiegant, and J M Hoovers, and N J Leschot
Institute of Human Genetics, University of Amsterdam, The Netherlands.

In first-trimester chorionic villus sampling (CVS) for prenatal diagnosis, abnormal chromosomal findings, such as mosaicism, trisomies, or suspect abnormal karyotypes, are found more frequently than at amniocentesis. The fact that these chromosomal abnormalities do not always reflect the fetal karyotype but may be restricted to the placenta is a major problem in diagnosis and counselling. In this paper we present the results of fluorescence in situ hybridization (FISH) studies on interphase nuclei of three term placentae investigated because of false-positive findings at first-trimester CVS. The chorionic villi of the first case showed a mosaic chromosome pattern involving a trisomy 10 cell line and a normal cell line, those of the second case a total trisomy 8 cell line, while in the third case a complete monosomy X was found. Follow-up amniocentesis in each of these three cases revealed a normal karyotype. By using FISH, we were able to confirm the presence of the aberrant cell lines, which were all confined to one part of the placenta. FISH on interphase nuclei allows the investigation of large numbers of cells for the existence of numerical chromosome aberrations in a quick and reliable way.

UI MeSH Term Description Entries
D007621 Karyotyping Mapping of the KARYOTYPE of a cell. Karyotype Analysis Methods,Analysis Method, Karyotype,Analysis Methods, Karyotype,Karyotype Analysis Method,Karyotypings,Method, Karyotype Analysis,Methods, Karyotype Analysis
D009030 Mosaicism The occurrence in an individual of two or more cell populations of different chromosomal constitutions, derived from a single ZYGOTE, as opposed to CHIMERISM in which the different cell populations are derived from more than one zygote.
D010920 Placenta A highly vascularized mammalian fetal-maternal organ and major site of transport of oxygen, nutrients, and fetal waste products. It includes a fetal portion (CHORIONIC VILLI) derived from TROPHOBLASTS and a maternal portion (DECIDUA) derived from the uterine ENDOMETRIUM. The placenta produces an array of steroid, protein and peptide hormones (PLACENTAL HORMONES). Placentoma, Normal,Placentome,Placentas,Placentomes
D011247 Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. Gestation,Pregnancies
D011263 Pregnancy Trimester, Third The last third of a human PREGNANCY, from the beginning of the 29th through the 42nd completed week (197 to 294 days) of gestation. Pregnancy, Third Trimester,Trimester, Third,Last Trimester,Last Trimesters,Pregnancies, Third Trimester,Pregnancy Trimesters, Third,Third Pregnancy Trimester,Third Pregnancy Trimesters,Third Trimester,Third Trimester Pregnancies,Third Trimester Pregnancy,Third Trimesters,Trimester, Last,Trimesters, Last,Trimesters, Third
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D015193 Chorionic Villi Sampling A method for diagnosis of fetal diseases by sampling the cells of the placental chorionic villi for DNA analysis, presence of bacteria, concentration of metabolites, etc. The advantage over amniocentesis is that the procedure can be carried out in the first trimester. Biopsy, Chorionic Villi,Chorionic Villus Sampling,Biopsies, Chorionic Villi,Chorionic Villi Biopsies,Chorionic Villi Biopsy,Chorionic Villi Samplings,Chorionic Villus Samplings,Sampling, Chorionic Villi,Sampling, Chorionic Villus,Samplings, Chorionic Villi,Samplings, Chorionic Villus
D017404 In Situ Hybridization, Fluorescence A type of IN SITU HYBRIDIZATION in which target sequences are stained with fluorescent dye so their location and size can be determined using fluorescence microscopy. This staining is sufficiently distinct that the hybridization signal can be seen both in metaphase spreads and in interphase nuclei. FISH Technique,Fluorescent in Situ Hybridization,Hybridization in Situ, Fluorescence,FISH Technic,Hybridization in Situ, Fluorescent,In Situ Hybridization, Fluorescent,FISH Technics,FISH Techniques,Technic, FISH,Technics, FISH,Technique, FISH,Techniques, FISH

Related Publications

G H Schuring-Blom, and M Keijzer, and M E Jakobs, and D M Van den Brande, and H M Visser, and J Wiegant, and J M Hoovers, and N J Leschot
January 1998, Cancer genetics and cytogenetics,
G H Schuring-Blom, and M Keijzer, and M E Jakobs, and D M Van den Brande, and H M Visser, and J Wiegant, and J M Hoovers, and N J Leschot
January 2010, Methods in molecular biology (Clifton, N.J.),
G H Schuring-Blom, and M Keijzer, and M E Jakobs, and D M Van den Brande, and H M Visser, and J Wiegant, and J M Hoovers, and N J Leschot
October 1996, Prenatal diagnosis,
G H Schuring-Blom, and M Keijzer, and M E Jakobs, and D M Van den Brande, and H M Visser, and J Wiegant, and J M Hoovers, and N J Leschot
August 1993, Genomics,
G H Schuring-Blom, and M Keijzer, and M E Jakobs, and D M Van den Brande, and H M Visser, and J Wiegant, and J M Hoovers, and N J Leschot
November 2005, Klinicheskaia laboratornaia diagnostika,
G H Schuring-Blom, and M Keijzer, and M E Jakobs, and D M Van den Brande, and H M Visser, and J Wiegant, and J M Hoovers, and N J Leschot
May 1998, BioTechniques,
G H Schuring-Blom, and M Keijzer, and M E Jakobs, and D M Van den Brande, and H M Visser, and J Wiegant, and J M Hoovers, and N J Leschot
January 2001, Genetics in medicine : official journal of the American College of Medical Genetics,
G H Schuring-Blom, and M Keijzer, and M E Jakobs, and D M Van den Brande, and H M Visser, and J Wiegant, and J M Hoovers, and N J Leschot
September 1995, International journal of urology : official journal of the Japanese Urological Association,
G H Schuring-Blom, and M Keijzer, and M E Jakobs, and D M Van den Brande, and H M Visser, and J Wiegant, and J M Hoovers, and N J Leschot
October 1992, Cancer genetics and cytogenetics,
G H Schuring-Blom, and M Keijzer, and M E Jakobs, and D M Van den Brande, and H M Visser, and J Wiegant, and J M Hoovers, and N J Leschot
July 2001, Virchows Archiv : an international journal of pathology,
Copied contents to your clipboard!