Molecular Human Reproduction, Vol. 8, No. 11, 1042-1045,
November 2002
© 2002 European Society of Human Reproduction and Embryology
Reproductive genetics |
X chromosome dosage by quantitative fluorescent PCR and rapid prenatal diagnosis of sex chromosome aneuploidies
1 Departament de Genética Molecular, General Lab, Barcelona 08021, 2 Unitat de Biologia, Departament de Biologia Cel·lular, Fisiologia i Immunologia, Universitat Autònoma de Barcelona E-08193 Bellaterra, Barcelona, Spain and 3 The Galton Laboratory and Department of Obstetrics and Gynaecology, University College London, London NW1 2HE, UK
During the past few years, rapid prenatal diagnosis of chromosome aneuploidies has been successfully achieved by quantitative fluorescent PCR (QF-PCR) amplification of chromosome-specific small tandem repeats (STR). This approach has proven to be very useful in clinical settings, since it allows the detection of major numerical disorders in a few hours after sampling. For the detection of Turners syndrome (45,X), several highly polymorphic STR on the X chromosome are needed in order to reduce the likelihood that a normal female might be homozygous for all sequences and, consequently, that the test could fail to discriminate between samples retrieved from a Turners and a normal female fetus. Here we report a new method for rapid and accurate detection of X chromosome copy number in prenatal samples that does not depend on STR heterozygosity. The test is based on QF-PCR amplification of the X-linked HPRT together with the autosomal D21S1411 used as internal control for quantification. In the course of this study, this assay allowed the prenatal diagnosis of a rare case of a normal female homozygous for four selected highly polymorphic X chromosome STR, as well as the assessment of the normal chromosome complement of a fetus homozygous for five chromosome 21 markers.
aneuploidy/prenatal diagnosis/QF-PCR/STR/Turners syndrome
4 To whom correspondence should be addressed at: Vincenzo Cirigliano, Genética Molecular, General Lab, c/Amigo 12, 08021 Barcelona, Spain. E-mail: v_cirigliano{at}hotmail.com
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