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Cargando
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Congress Venue: Palau de Congressos de Catalunya
Avinguda Avinguda Diagonal 661 - 671
08028 Barcelona
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Wednesday, April 23rd 2008
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| 09:00 - 09:30 |
Open Ceremony
The Origin of human aneuploidy: Where we have been, where we are going
Chairman: S. Munné
T. Hassold |
| 09:30 - 11:00 |
SESSION 1. From Prenatal to PGD
Moderators: J.L. Simpson, A. Fortuny
PND or PGD: Helping patients make sense out of genetic risk
The-Hung Bui
Biochips for PND
Luis A. Pérez Jurado
Molecular methods for Prenatal Diagnosis and future implications
C. Vincenzo
The place of PGD in Human Medicine
J.L. Simpson
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| 11:00 - 11:30 |
Coffee break |
| 11:30 - 12:45 |
SESSION 2. PGD: technical aspects
Moderators: M. Sandalinas, M. Florensa
Embyo biopsy
J. Cohen
Embryo cryopreservation in PGD
M. Boada
Mosaicism and/or error rate
S. Munné
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| 12:40 - 14:00 |
Free communications 1
Moderators: C. Magli, M. Florensa
Rapid PND of common chromosome aneuploidies by QF-PCR. Large sacleclinical application and future implications
Molecular diagnostics of Down syndrome using quantitative APEX microarrays |
| (Oitmaa , E Tartu , Estonia) |
| Benefit of preimplantation genetic screening is related to improved laboratory practice |
| (Beyer, C , ) |
| A review of blastocyst biopsy outcomes from routine clinical application in over 1100 cycles |
| (Traversa , M.V Sydney, Australia) |
| monosomy rescue in preimplantation genetic diagnosis of aneuploidy. |
| (Colls , P Livingston, United States) |
| The use of telomeric probes in PGS - selecting categories for which it has the biggest benefit |
| (Baborova , P Pilsen, Czech Republic) |
| DNA fragmentation and aneuploidy rates in the sperm of infertile men before and after density gradient centrifugation (DGC). |
| (Christopikou, D Marousi, Greece) |
| Survival of frozen-thawed blastocysts after preimplantatio genetic diagnosis: Pregnancy and delivery |
| (Hernández , J La Laguna, Spain) |
|
| 12:40 - 14:00 |
Genetic Analysis in ART. Symposium for IVF practitioners
Moderator: E. Hernández
How to prepare an IVF-PGD cycle
M. Sánchez
Relevance of karyotyping and genetic counselling in an IVF program
M. del Campo
PND in an IVF program
V. Cirigliano
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| 14:00 - 15:00 |
Lunch
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| 15:00 - 16:30 |
SESSION 3. PGD for infertility I: AMA, RPL, MALE
Moderator: S. Munné, Y. Verlinsky
Advance maternal age
C. Maglí
Repeated pregnancy loss
C. Rubio
Severe male infertility
S. Kahraman
Repeated implantation failure
L. Wilton
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| 16:30 - 17:00 |
Coffee break |
| 17:00 - 18:40 |
Free communications 2
Moderators: S. Munné, I. Tur-Kaspa
| Human susceptibility to aneuploidy and the link to infertility |
| (Mantzouratou , A London, United Kingdom) |
| Number of oocytes retrieved and cycle outcome in preimplantation genetic diagnosis (pgd) patients for aneuplody screening |
| (Santana Martín, A Valencia, Spain) |
| Incidence of embryo aneuploidies in two hormonal stimulation protocols |
| (Mercader , A Valencia, Spain) |
| Diagnosis of the male factor: an important step towards optimizing pregnancy rates in art |
| (Velilla , E Barcelona, Spain) |
| Relationship between sperm aneuploidy and pgd |
| (Sánchez , M Barcelona, Spain) |
| Impact of sperm chromosomal abnormalities on the chromosomal constitution of preimplantation embryos |
| (Rodrigo , L Valencia, Spain) |
| Preimplantation genetic diagnosis significantly reduces pregnancy loss and increases implantation rate in poor prognosis patients |
| (Kavrut , M , Turkey) |
| Is preimplantation genetic screening useful in repeated IVF failure group ? |
| (gordts , s Leuven, Belgium) |
| Beneficial effects of preimplantation genetic diagnosis in patients with repeated implantation failures |
| (Beyazyurek , C Istanbul, Turkey) |
| Aneuploidy preimplantation genetic screening for patients presenting with recurrent pregnancy loss. |
| (Leigh, D.A Sydney, Australia) |
|
| 20:00 |
Welcome Reception |
Thursday, April 24th 2008
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| 09:00 - 09:30 |
General Interest Lecture 1
Preimplantation Genetic Diagnosis in Europe
Chairman: J.L. Simpson
D. Ibarreta
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| 09:30 - 11:00 |
SESSION 4. PGD for chromosomal rearrangements
Moderators: A. Kuliev, L.Gianaroli
PGD vs. PND for Robertsonian and reciprocal translocation
A. Handyside
Results and Follow up
J. Fischer
Chromosomal rearrangements and male infertility
E. Antón
Interchromosomal effects. Studies on sperm
R. Martin
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| 11:00 - 11:30 |
Coffee break |
| 11:30 - 12:45 |
SESSION 5. Alternatives for Embryo Selection
Moderators: J. Cohen, D. Cram
Alternatives for Embryo Selection
J. Cohen
Human endometrial receptivity
F. Domínguez
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| 12:40 - 14:00 |
Free communications 3
Moderators: J. Cohen, A. Kuliev
| Cytogenetic studies of first trimester spontaneous miscarriage: what relevance to pgd/pgs? |
| (Hardy , K Bentley, Australia) |
| The meiotic segregation of paracentric inversions: how breakpoint mapping can make the difference |
| (Pellestor , F Montpellier, France) |
| Reproductive relevance of chromosomal aberrations in male karyotypes |
| (Bronet , F Madrid, Spain) |
| Outcomes of preimplantation genetic diagnosis cycles for translocation carriers: 8-year experience |
| (Beyazyurek , C Istanbul, Turkey) |
| Preimplantation genetic diagnosis in translocations carriers |
| (parriego , M , Spain) |
| Preimplantation genetic diagnosis for reciprocal translocationas, japanease experience |
| (Muriel, Roche , ) |
| Can high magnification morphological selection of spermatozoa be effective reducing chromosomal risk for patients carrying translocations ? |
| (Vialard , F Poissy, France) |
| Predictive value of embryo morphology on day-3 and day-5 in chromosomal abnormalities of older patients. |
| (Florensa , M , Spain) |
|
| 12:40 - 14:00 |
Genetic Analysis in ART. Symposium for IVF practitioners
Moderator: X. Nadal
Dilemnas in male factor: Role of aneuploidy analysis in male infertility
L. Gianaroli
Meiosis study in testicular biopsy
Z. Sarrate
Sperm genetic analysis in patient with altered karyotype
J. Blanco
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| 14:00 - 15:00 |
Lunch
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| 15:00 - 16:30 |
SESSION 6. PGD for infertility III: CGH & arrays
Moderator: L. Wilton, J. Martin
Clinical application of new strategies for preimplantation genetic screening employing CGH
D. Wells
M. Hughes
Application of array-CGH in PGD aneuploidy screening
A. Hellani
Genetics and "omics"
E. Fragkouli
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| 16:30 - 17:00 |
Coffee break |
| 17:00 - 18:40 |
Free Communications 4
Moderators: D. Wells, M. Hughes
| Comprehensive microarray genetic analyses on single cells from human embryos to determine 23-chromosome aneuploidy, structural chromosome aberrations, and genome-wide scans using single nucleotide polymorphisms (SNPs); to identify what partner provided the extra chromosome in aneuploid embryos; and to determine what embryo implanted following an in vitro fertilization (IVF) cycle. |
| (Kearns, W.G rockville, United States) |
| 24 Chromosome Screening in Single Cells using Microarray Comparative Genomic Hybridization Methods: Implications for Preimplantation Genetic Diagnosis. |
| (Steuerwald , N.M , United States) |
| Beta Thalassemia with HLA Typing for PGD |
| (Ozgon , G Istanbul, Turkey) |
| Double Factor Preimplantation Genetic Diagnosis applied to Angelman Syndrome. |
| (Obradors , A Bellaterra, Spain) |
| Preimplantation Genetic Diagnosis for Zellweger Syndrome |
| (Barsky , I Chicago, United States) |
| Preimplantation Genetic Diagnosis (PGD) in a highly recombinant region: when crossover between the TSC2 gene and linked markers makes accurate diagnosis extremely difficult |
| (Renbaum , P Jerusalem, Israel) |
| Preimplantation diagnosis for mitochondrial DNA disorders: contribution to understanding mitochondrial DNA segregation during early human embryonic development |
| (Steffann Julie, J Paris, France) |
| Preimplantation genetic diagnosis of single gene disorders: outcome from over 200 cases |
| (Sanchez Garcia , J.F Livingston, United States) |
| Multiple displacement amplification (mda) in preimplantation genetic diagnosis (pgd): bernabeu institute experience. |
| (Lledo , B Alicante, Spain) |
| Patients' experiences of Preimplantation Genetic Diagnosis (PGD) in Sweden |
| (Malmgren , H Stockholm, Sweden) |
|
| 09:00 - 09:30 |
General Interest Lecture 2
Reproductive Genetics and Future Evolution of the Human Species
Chairman: M. Hughes
L. Silver
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| 09:30 - 11:00 |
SESSION 7. PGD for gene defects
Moderators: D. Wells, C. Giménez
Preimplantation genetic diagnosis for late onset diseases
C. Spits
Preimplantation HLA typing
S. Rechitsky
PGD for gene defects in blastocyst stage
G. Kokkali
Choosing disability PGD and negative enhancement I
I. Karpin
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| 11:00 - 11:30 |
Coffee break |
| 11:30 - 12:45 |
SESSION 8. PGD ART DATA & SAFETY. EPIGENETICS
Moderator: J.L. Simpson, S. Kahraman
ESHRE DATA
J. Harper
Clinical Outcome of PGD
I. Tur-Kaspa
Epigenetics and male infertility
C. Camprubí
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| 12:40 - 14:00 |
Free communications 5
Moderators: S. Rechitsky, J. Martín
| Characterizations of the post-pgd embryo– the laws and policies of four countries |
| (van Wagner, E.) |
| Clinical outcome of newborn and child development follow-up: ivf vs ivf-pgd cyclesC |
| (Velilla Garcia, E Barcelona, Spain) |
| Public awareness and regulation of preimplantation genetic diagnosis in australia |
| (van Leeuwen , B Canberra, Australia) |
| French national cohort of children born after pgd |
| (Foix-L'Hélias Foix-Hélias, L Clamart, France) |
| The European Human Embryonic Stem Cell Registry-hESCreg |
| (Aran , B Barcelona, Spain) |
| Derivation and characterization of the first abnormal human embryonic stem cell carrying a mutated Von Hippel Lindau (VHL) allele |
| (De Vos , J Montpellier, France) |
| Chromosomes from embryonic cells: A cytogenetic analysis. |
| (Leigh, D Sydney, Australia) |
| Blastocysts derived from low and high quality embryos are equally potential sources of human embryonic stem cells lines establishment |
| (Borges Jr., E.B Sao Paulo, Brazil) |
|
| 12:40 - 14:00 |
Genetic Analysis in ART. Symposium for IVF practitioners
Moderator: A. Palumbo
Optimization of ovarian estimulation for PGD
I. Tur-Kaspa
When to cancel PGD
G. Calderón
Embryo transfer in biopsied embryos
B. Coroleu
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| 14:00 - 15:00 |
Lunch
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| 15:00 - 15:30 |
General Interest Lecture 3
The ethics of using embryos in research
Chairman: C. Simón
G. Pennings
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| 15:30 - 16:30 |
SESSION 9. STEM CELLS & ART
Moderator: C. Simón, E. Ibáñez
Merging ART and Stem cells
D. Cram
PGD as a source of hESC lines with genetic conditions
Y. Verlinsky
Stem cells and regenerative medicine
A. Raya
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| 16:30 - 17:00 |
Closing Ceremony. Award in memory of Dr. Josep Egozcue to the best presented abstract
Chairmen: S. Munné, A. Kuliev |
Saturday, April 26th 2008
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Open Forum - Meet the Experts - Session for Patients
Jornada de Portes Obertes - Jornada de Puertas Abiertas |
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A reality that gives hope for the prevention of genetic diseases:
Preimplantation Genetic Diagnosis
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Venue: CaixaForum
Avinguda Marquès De Comillas 6-8
08038 Barcelona
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| 09:00 - 09:30 |
Documentation pick up |
| 09:30 - 10:00 |
Introduction
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| 10:00 - 10:50 |
SESSION I: GENETIC AND HEREDITARY DISEASES |
| 10:00 - 10:15 |
Genetic Counsel
Luis A. Pérez Jurado
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| 10:15 - 10:30 |
Mucopolysaccharidosis: personal experience
Mercè López
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| 10:30 - 10:50 |
General discussion
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| 10:50 - 11:10 |
Coffee break |
| 11:10 - 12:30 |
SESSION II. PREIMPLANTATION GENETIC DIAGNOSIS FOR HEREDITARY DISEASES |
| 11:10 - 11:25 |
PGD for monogeneic diseases
Mark Hughes
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| 11:25 - 11:40 |
HLA and genetic diseases
Dagan Wells
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| 11:40 - 11:55 |
Setting up a PGD Protocol
Julio Martín
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| 11:55 - 12:10 |
Fanconi Anemia: personal experience
Salvador Moreno
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| 12:10 - 12:30 |
General discussion |
| 12:30 - 13:35 |
SESSION III. STEM CELLS AND GENETIC DISEASES |
| 12:30 - 12:45 |
PGD as a source of HeSC lines with genetic conditions
David Cram
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| 12:45 - 13:00 |
Cellular therapy and genetic for genodermatosis
Marcela del Río
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13:00 - 13:15
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Epidermiolysis Bullosa patient
Lucía Tevar
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| 13:15 - 13:35 |
General discussion |
| Poster logistics |
| Set up |
Wednesday, 23rd from 10.00 hours |
| Dismantle |
Friday, 25th at 15.00 hours |
| Measures |
90 centimetres width per 120 centimetres high |
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Number
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Title
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0.001 |
Canada’s national citizen deliberation on preimplantation genetic diagnosis |
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0.002 |
Preimplantation genetic diagnosis on the social determinants of the “health” of embryos |
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4.001 |
Twin pregnancy after double factor pgd analysis: diagnosis of von hippel-lindau disease and aneuploidy screening. |
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4.002 |
Genetic aspects of male infertility in art |
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4.003 |
The use of fastfish for preimplantation genetic screening |
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4.004 |
New approaches in polar body analysis |
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5.001 |
Origin of autosomal monosomy in early stages of preimplantation embryo development |
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5.002 |
Aneuploidy levels in blood cells and oocytes |
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5.003 |
Prognosis of preimplantation genetic diagnosis in oncologic patients |
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5.004 |
Improvement of chances by preimplantation genetic screening |
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5.005 |
Morphology embryo selection: does we work correctly in recurrent miscarriage couples? |
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5.006 |
Clinical pregnancy and live birth rates in women >=38 years old undergoing ivf with and without pgd |
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5.007 |
Clinical outcome of preimplantation genetic diagnosis for aneuploidy screening in couples with recurrent miscarriage: the mexican experience |
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5.008 |
Development of a single cell pcr protocol for the detection of myotonic dystrophy,sex and chromosome 21 copy number |
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6.001 |
Sperm fish analysis of a familial complex chromosome rearrangement (ccr): predictive value on the outcome of preimplantation genetic diagnosis (pgd) |
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6.002 |
Case report: meiotic segregation pattern and preimplantation diagnosis in a robertsonian translocation (13;21) |
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6.003 |
Fish analysis of chromosome segregation in sperm of a t(1;15)(q21;p12) carrier: predictive test for pgd. |
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6.004 |
Case report: normal birth after preimplantation genetic diagnosis by fish in a couple with a balanced translocation der(15)t(y;15)(p12;p11.1) associated with severe oligoastenospermia and testicular seminoma in the male partner. |
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6.005 |
Preimplantation genetic testing outcomes for poor prognosis cryptic translocation carrier couples |
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7.001 |
One-step multiplex pcr for preimplantation genetic diagnosis of huntington's disease. |
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7.002 |
Preimplantation genetic diagnosis for hypophosphatasia. |
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7.003 |
Successful outcomes in thirty six cycles of preimplantation genetic diagnosis for twelve kinds of single gene disorders |
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7.004 |
Preimplantation genetic diagnosis for nonsyndromic deafness by polar body and blastomere biopsy |
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7.005 |
A de novo factor viii (f8) mutation creates a challenge for pgd |
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7.006 |
Application of pgd for single gene disorders |
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7.007 |
A new approach for haplotyping single gene pgd in couples with de novo mutations. |
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7.008 |
Fully informative preimplantation genetic diagnosis for cystic fibrosis in a couple with an unknown maternal mutation using microsatellite markers |
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7.009 |
Term pregnancies after pgd for portuguese familial amyloidotic polyneuropathy |
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7.010 |
Preimplantation genetic diagnosis of cytochrome c oxidase deficiency (cox) |
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7.011 |
Successful preimplantation genetic diagnosis for duchenne muscular dystrophy using multiple displacement amplification |
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7.012 |
Outcome of preimplantation genetic diagnosis for genetic disease |
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7.013 |
Preimplantation genetic diagnosis for familial hypercholesterolaemia |
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7.014 |
Pgd is a valuable reproductive option for couples at risk of transmitting autosomal dominant disorders with high clinical variability |
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7.015 |
Molecular analysis of sma for preimplantation genetic diagnosis |
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7.016 |
Newborn children after preimplantational genetic diagnosis in an affected couple with x-linked adrenoleukodystrophy. |
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7.017 |
Y chromosome microdeletions in iranian infertile men |
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7.018 |
Outcomes of Preimplantation genetic diagnosis for single gene disorders |
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9.001 |
Blastocyst biopsy- evaluation of data 4 years on |
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9.002 |
Vitrification of biopsied blastocysts using a closed method |
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9.003 |
Preimplantation genetic aneuploidy screening in women older than 42 years |
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9.004 |
Preimplantation genetic diagnosis in a public hospital in spain. an alternative to prenatal diagnosis |
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10.001 |
Elucidation of abnormal fertilization by single cell analysis using fish and pcr haplotype analysis |
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11.001 |
Influence of the fertilization procedure on pgd cycles outcomes in absense of male factor |
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11.002 |
Embryo development and aneuploidy rate of multinucleated embryos from an donor egg ivf program |
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11.003 |
Developmental competence of fresh and frozen-thawed embryos after biopsy of two blastomeres in preimplantation genetic diagnosis |
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11.004 |
Pregnancy of transgenic-clone goat using mammary gland epithelial cells as donor cells |
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14.002 |
Olygohydramnios diagnosis treatment and consequences in term and postterm pregnancies |
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15.001 |
Blastocyst biopsy in pgd practice: laboratory considerations |
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.JPG)
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