Literature DB >> 17192963

Preimplantation genetic diagnosis for myotonic dystrophy type 1: detection of crossover between the gene and the linked marker APOC2.

Georgia Kakourou1, Seema Dhanjal, Danny Daphnis, Alpesh Doshi, Sarah Nuttall, Sarah Gotts, Paul Serhal, Joy Delhanty, Joyce Harper, Sioban SenGupta.   

Abstract

OBJECTIVE: To report two cases of preimplantation genetic diagnosis (PGD) for myotonic dystrophy type I (DM1) where cross-over between the DMPK locus and a linked polymorphic marker APOC2 was detected.
METHODS: Embryos from in vitro fertilisation (IVF) were biopsied at day 3 of development and single blastomeres collected. Diagnosis was performed by duplex or triplex fluorescent-polymerase chain reaction (F-PCR) to amplify DMPK and APOC2 loci, or DMPK with APOC2 and D19S112 polymorphic markers.
RESULTS: A total of 22 oocytes were retrieved from the two patients, 20 were inseminated of which 15 fertilized (75%) and were suitable for biopsy on day 3. A diagnosis was obtained for 12 embryos (80%) and was confirmed in all un-transferred embryos. Crossover between DM1 and APOC2 was detected in two embryos from the two different couples. Transfer of two embryos took place in both cases resulting in two pregnancies. Each couple have had a healthy baby.
CONCLUSION: The above cases highlight the importance of using more than one linked polymorphic marker in PGD-PCR protocols and emphasize the danger of using APOC2 as the sole marker to identify the DM1 mutation. (c) 2006 John Wiley & Sons, Ltd.

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Year:  2007        PMID: 17192963     DOI: 10.1002/pd.1611

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  8 in total

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2.  The clinical application of preimplantation genetic diagnosis for the patient affected by congenital contractural arachnodactyly and spinal and bulbar muscular atrophy.

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3.  Familial haplotyping and embryo analysis for Preimplantation genetic diagnosis (PGD) using DNA microarrays: a proof of principle study.

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4.  Preimplantation genetic diagnosis (PGD) for nonsyndromic deafness by polar body and blastomere biopsy.

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Journal:  J Assist Reprod Genet       Date:  2009-07       Impact factor: 3.412

5.  Preimplantation genetic diagnosis: its role in prevention of deafness.

Authors:  M K Taneja
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2014-02-20

6.  The impact of parental unaffected allele combination on the diagnostic outcome in the preimplantation genetic testing for myotonic dystrophy type 1 in Japanese ancestry.

Authors:  Hiroshi Senba; Kou Sueoka; Suguru Sato; Nobuhiko Higuchi; Yuki Mizuguchi; Kenji Sato; Mamoru Tanaka
Journal:  Reprod Med Biol       Date:  2020-04-29

7.  Preimplantation genetic diagnosis and deafness.

Authors:  M K Taneja
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2012-06-30

8.  A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran.

Authors:  Marzieh Mojbafan; Sirous Zeinali; Yeganeh Keshvar; Solmaz Sabeghi; Zohreh Sharifi; Kiyana Sadat Fatemi; Panti Fouladi; Shahrzad Younesi Khah; Faezeh Rahiminejad; Atefeh Joudaki; Masoume Amini; Hamideh Bagherian; Marefat Ghaffari Novin; Mansoureh Movahedin
Journal:  BMC Pregnancy Childbirth       Date:  2022-04-15       Impact factor: 3.007

  8 in total

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