Document Detail


What do French patients and geneticists think about prenatal and preimplantation diagnoses in Marfan syndrome?
MedLine Citation:
PMID:  23147988     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
OBJECTIVES: Marfan syndrome (MFS) is an autosomal dominant connective tissue disorder with manifestations mainly involving the skeletal, ocular, and cardiovascular systems. The phenotypic variability observed in MFS makes genetic counselling difficult. Prenatal diagnosis (PND) and preimplantation genetic diagnosis are technically feasible when a causal mutation is identified, but both raise many ethical questions in this condition. Little is known about opinions and practices in such reproductive issues in MFS. The goal of this study was to report on patients' points of view and geneticists' standard practices. METHODS: Two different questionnaires were produced. RESULTS: Fifty geneticists filled in the questionnaire. Twenty-two per cent thought that PND was acceptable, 72% debatable and 6% not acceptable. Preimplantation genetic diagnosis was more often reported acceptable (34% of answers). Results varied according to the physician's experience with the disease. Fifty-four answers were collected for patients' questionnaires. Most of them (74%) were favourable to the development of prenatal testing, and believed that the choice should be given to parents. However, only a minority would opt for prenatal diagnosis for themselves. CONCLUSION: This study showed that the majority of patients were in favour of PND and that opinions among practitioners varied widely, but that overall, practitioners favoured a systematic multidisciplinary evaluation of the couple's request. © 2012 John Wiley & Sons, Ltd.
Authors:
F Coron; T Rousseau; G Jondeau; E Gautier; C Binquet; L Gouya; V Cusin; S Odent; Y Dulac; H Plauchu; P Collignon; M-A Delrue; B Leheup; L Joly; F Huet; J Thevenon; G Mace; C Cassini; C Thauvin-Robinet; J E Wolf; N Hanna; P Sagot; C Boileau; L Faivre
Related Documents :
24468978 - Pre-operative role of braf in the guidance of the surgical approach and prognosis of di...
8627538 - Evaluation of potential genetic associations between ethanol tolerance and sensitizatio...
17171388 - Behavioral genomics of honeybee foraging and nest defense.
24307908 - Do not be fooled by fancy mutations: inflammatory fibroid polyps can harbor mutations s...
14574828 - Genetic and neurodevelopmental influences in autistic disorder.
18947448 - Landscape composition modulates population genetic structure of eriosoma lanigerum (hau...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-11-13
Journal Detail:
Title:  Prenatal diagnosis     Volume:  -     ISSN:  1097-0223     ISO Abbreviation:  Prenat. Diagn.     Publication Date:  2012 Nov 
Date Detail:
Created Date:  2012-11-13     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8106540     Medline TA:  Prenat Diagn     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
© 2012 John Wiley & Sons, Ltd.
Affiliation:
Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, France.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Effects-based marine ecological risk assessment at a polychlorinated biphenyl-contaminated site in S...
Next Document:  Ruthenium-Catalyzed Reductive Coupling of 1,3-Enynes and Aldehydes by Transfer Hydrogenation: anti-D...