Literature DB >> 30891099

Clinical experience with multiplex ligation-dependent probe amplification for microdeletion syndromes in prenatal diagnosis: 7522 pregnant Korean women.

Dongsook Lee1,2, Sohyun Na1, Surim Park1, Sanghee Go1, Jinyoung Ma1, Soonha Yang1, Kichul Kim1, Seunggwan Lee2, Doyeong Hwang1.   

Abstract

BACKGROUND: Conventional cytogenetic analysis using G-band karyotyping has been the method of choice for prenatal diagnosis, accurately detecting chromosomal abnormalities larger than 5 Mb. However, the method is inefficient for detecting the submicroscopic deletions and duplications that are associated with malformations and mental retardation. This study evaluated the results of the multiplex ligation-dependent probe amplification (MLPA) P245 assay used for prenatal diagnosis in cases with unusual ultrasonographic findings or specifically where parents wanted to be tested. The objective was to compare the results from MLPA with those from conventional cytogenetic testing in order to determine their concordance and the additional diagnostic yield of MLPA over G-band karyotyping.
RESULTS: Of the 7522 prenatal cases analyzed, 124 were found to have genomic imbalances (1.6%). Of those 124 cases, 41 had gene loss (33.6%), and 83 had gene gain (66.4%). Most of the cases with genomic imbalances (64.5%) showed no abnormal karyotype. In particular, all cases with a 4p16.3 deletion (Wolf-Hirschhorn syndrome) showed an abnormal karyotype, whereas all of those with a 22q11-13 deletion showed a normal karyotype. In most of the cases with pathogenic deletions, the indication for invasive prenatal testing was an increase in the nuchal translucency (NT) alone (51.2%). Other indications observed in the remaining cases were abnormal serum screening markers (14.6%), other ultrasonographic findings (9.8%), pregnancy through in vitro fertilization and fertility assistance (9.8%), and advanced maternal age(2.4%).
CONCLUSIONS: These results show that for fetuses with an enlarged NT or abnormal ultrasonographic findings and normal conventional karyotype, additional genetic investigation like molecular testing would be for identifying the microscopic genomic aberrations (microdeletions, microduplications) responsible for syndromic associations including structural anomalies and mental retardation.

Entities:  

Keywords:  Increased nuchal translucency; MLPA P245; Microdeletion syndromes; Multiplex ligation-dependent probe amplification (MLPA); Prenatal diagnosis

Year:  2019        PMID: 30891099      PMCID: PMC6390335          DOI: 10.1186/s13039-019-0422-8

Source DB:  PubMed          Journal:  Mol Cytogenet        ISSN: 1755-8166            Impact factor:   2.009


  34 in total

1.  Partial deletion of 4p and 4q in a fetus with ring chromosome 4: phenotype and molecular mapping of the breakpoints.

Authors:  A Kocks; S Endele; R Heller; B Schröder; H-J Schäfer; C Städtler; M Makrigeorgi-Butera; A Winterpacht
Journal:  J Med Genet       Date:  2002-05       Impact factor: 6.318

2.  Rapid, high throughput prenatal detection of aneuploidy using a novel quantitative method (MLPA).

Authors:  H R Slater; D L Bruno; H Ren; M Pertile; J P Schouten; K H A Choo
Journal:  J Med Genet       Date:  2003-12       Impact factor: 6.318

3.  Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome.

Authors:  Svetlana A Yatsenko; Ellen K Brundage; Erin K Roney; Sau Wai Cheung; A Craig Chinault; James R Lupski
Journal:  Hum Mol Genet       Date:  2009-03-17       Impact factor: 6.150

Review 4.  Increased nuchal translucency in euploid fetuses--what should we be telling the parents?

Authors:  C M Bilardo; E Timmerman; E Pajkrt; M van Maarle
Journal:  Prenat Diagn       Date:  2010-02       Impact factor: 3.050

5.  Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow.

Authors:  Malgorzata Srebniak; Marjan Boter; Grétel Oudesluijs; Marieke Joosten; Lutgarde Govaerts; Diane Van Opstal; Robert-Jan H Galjaard
Journal:  Eur J Hum Genet       Date:  2011-06-22       Impact factor: 4.246

6.  Nuchal translucency and congenital heart defects: heart failure or not?

Authors:  J M Simpson; G K Sharland
Journal:  Ultrasound Obstet Gynecol       Date:  2000-07       Impact factor: 7.299

7.  8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families.

Authors:  John Ck Barber; Dave Bunyan; Merryl Curtis; Denise Robinson; Susanne Morlot; Anette Dermitzel; Thomas Liehr; Claudia Alves; Joana Trindade; Ana I Paramos; Clare Cooper; Kevin Ocraft; Emma-Jane Taylor; Viv K Maloney
Journal:  Mol Cytogenet       Date:  2010-02-18       Impact factor: 2.009

8.  Increased nuchal translucency thickness and normal karyotype: time for parental reassurance.

Authors:  C M Bilardo; M A Müller; E Pajkrt; S A Clur; M M van Zalen; E K Bijlsma
Journal:  Ultrasound Obstet Gynecol       Date:  2007-07       Impact factor: 7.299

9.  Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms.

Authors:  H L Wilson; A C C Wong; S R Shaw; W-Y Tse; G A Stapleton; M C Phelan; S Hu; J Marshall; H E McDermid
Journal:  J Med Genet       Date:  2003-08       Impact factor: 6.318

10.  Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations.

Authors:  Paola Evangelidou; Carolina Sismani; Marios Ioannides; Christodoulos Christodoulou; George Koumbaris; Ioannis Kallikas; Ioannis Georgiou; Voula Velissariou; Philippos C Patsalis
Journal:  Mol Cytogenet       Date:  2010-11-26       Impact factor: 2.009

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