Éditeur(s) : Université de Guyane
Extrait de : "Bals masqués de Guyane et d'ailleurs. Identités et imaginaires carnavalesques en question" : colloque international, les 26 et 27 janvier 2017. Université de Guyane
Description : Différence entre les bals masqués d'ailleurs et les bals paré-masqués de Guyane. Le bal paré-masqué de Guyane renvoi à la séduction du touloulou par le costume qu'il porte, il est dans l'exhibition. Il comporte un avant, un pendant, et un après dancing. Les femmes se préparent et vont se retrouver dans la plus grande discrétion, pour préparer leurs toilettes, s'habiller ensemble, vont être marrainées avec quelqu'un de plus âgé qui leurs transmettent les codes, les symboles, les rites : l'anonymat, l'anonymat à travers le vêtement, le parlé, la démarche...etc. Le bal paré-masqué de Guyane, c'est tout un ensemble de rite, ce qui le distingue des autres bals masqués d'ailleurs.
Siècle(s) traité(s) : 20
Droits : CC-BY-NC-ND - Attribution - Pas d'utilisation commerciale - Pas de modification
Permalien : http://www.manioc.org/fichiers/V17169
V17169

Éditeur(s) : Université de Guyane
Extrait de : "Bals masqués de Guyane et d'ailleurs. Identités et imaginaires carnavalesques en question" : colloque international, les 26 et 27 janvier 2017. Université de Guyane
Description : Première romancière guyanaise Lyne Marie Stanley "La saison des abattis" (1996) à Cayenne. La fête danser costumer et masqué à nourri l'imaginaire des auteurs et de leur protagoniste. La salle de bal est souvent décrite comme un lieu mythique, mystérieux propice aux rêves aux intrigues amoureuses, aux rencontres fatales. Lyne Marie Stanley dans "La saison des abattis", dans le chap. 3, s'attache à présenter le bal paré-masqué des "touloulous" : personnage féminin emblématique du carnaval de Guyane. Céphyse, "touloulou" novice découvre l'univers du bal paré-masqué en même temps que l'amour. Elle transgresse les codes établies qui consistent en autre à préserver l?anonymat. La première fonction du déguisement est de garantir l'anonymat du "touloulou" personnage unique du carnaval guyanais." Le frère du "touloulou" est le "tololo" qui signifie en créole guyanais : "ton pénis" Le rôle essentiel de la parade du touloulou est sans doute, de mettre en valeur la femme, de la magnifier, pour en faire un personnage sublimée, à la fois réelle et virtuelle. La représentation du bal paré-masqué dans : "La saison des abattis", est une excellente illustration du concept de transgression, dans le cadre de la fête carnavalesque guyanaise. Pour Jean Thierry Martins, le bal masqué est dans tous les cas un lieu de transgression sémantique.
Siècle(s) traité(s) : 20
Droits : CC-BY-NC-ND - Attribution - Pas d'utilisation commerciale - Pas de modification
Permalien : http://www.manioc.org/fichiers/V17167
V17167

Éditeur(s) : HAL CCSD
Résumé : International audience
Up-to-date estimates of the health outcomes of preterm children are needed for assessing perinatal care, informing parents, making decisions about care, and providing evidence for clinical guidelines. To determine survival and neonatal morbidity of infants born from 22 through 34 completed weeks' gestation in France in 2011 and compare these outcomes with a comparable cohort in 1997. The EPIPAGE-2 study is a national, prospective, population-based cohort study conducted in all maternity and neonatal units in France in 2011. A total of 2205 births (stillbirths and live births) and terminations of pregnancy at 22 through 26 weeks' gestation, 3257 at 27 through 31 weeks, and 1234 at 32 through 34 weeks were studied. Cohort data were collected from January 1 through December 31, 1997, and from March 28 through December 31, 2011. Analyses for 1997 were run for the entire year and then separately for April to December; the rates for survival and morbidities did not differ. Data are therefore presented for the whole year in 1997 and the 8-month and 6-month periods in 2011. Survival to discharge and survival without any of the following adverse outcomes: grade III or IV intraventricular hemorrhage, cystic periventricular leukomalacia, severe bronchopulmonary dysplasia, retinopathy of prematurity (stage 3 or higher), or necrotizing enterocolitis (stages 2-3). A total of 0.7% of infants born before 24 weeks' gestation survived to discharge: 31.2% of those born at 24 weeks, 59.1% at 25 weeks, and 75.3% at 26 weeks. Survival rates were 93.6% at 27 through 31 weeks and 98.9% at 32 through 34 weeks. Infants discharged home without severe neonatal morbidity represented 0% at 23 weeks, 11.6% at 24 weeks, 30.0% at 25 weeks, 47.5% at 26 weeks, 81.3% at 27 through 31 weeks, and 96.8% at 32 through 34 weeks. Compared with 1997, the proportion of infants surviving without severe morbidity in 2011 increased by 14.4% (P < .001) at 25 through 29 weeks and 6% (P < .001) at 30 through 31 weeks but did not change appreciably for those born at less than 25 weeks. The rates of antenatal corticosteroid use, induced preterm deliveries, cesarean deliveries, and surfactant use increased significantly in all gestational-age groups, except at 22 through 23 weeks. The substantial improvement in survival in France for newborns born at 25 through 31 weeks' gestation was accompanied by an important reduction in severe morbidity, but survival remained rare before 25 weeks. Although improvement in survival at extremely low gestational age may be possible, its effect on long-term outcomes requires further studies. The long-term results of the EPIPAGE-2 study will be informative in this regard.
ISSN: 2168-6211

hal-01258705
http://hal.univ-brest.fr/hal-01258705
PUBMED : 25621457
DOI : 10.1001/jamapediatrics.2014.3351

Éditeur(s) : HAL CCSD
Résumé : International audience
Background Orodental diseases include several clinically and genetically heterogeneous disorders that can present in isolation or as part of a genetic syndrome. Due to the vast number of genes implicated in these disorders, establishing a molecular diagnosis can be challenging. We aimed to develop a targeted next-generation sequencing (NGS) assay to diagnose mutations and potentially identify novel genes mutated in this group of disorders. Methods We designed an NGS gene panel that targets 585 known and candidate genes in orodental disease. We screened a cohort of 101 unrelated patients without a molecular diagnosis referred to the Reference Centre for Oro-Dental Manifestations of Rare Diseases, Strasbourg, France, for a variety of orodental disorders including isolated and syndromic amelogenesis imperfecta (AI), isolated and syndromic selective tooth agenesis (STHAG), isolated and syndromic dentinogenesis imperfecta, isolated dentin dysplasia, otodental dysplasia and primary failure of tooth eruption. Results We discovered 21 novel pathogenic variants and identified the causative mutation in 39 unrelated patients in known genes (overall diagnostic rate: 39%). Among the largest subcohorts of patients with isolated AI (50 unrelated patients) and isolated STHAG (21 unrelated patients), we had a definitive diagnosis in 14 (27%) and 15 cases (71%), respectively. Surprisingly, COL17A1 mutations accounted for the majority of autosomal-dominant AI cases. Conclusions We have developed a novel targeted NGS assay for the efficient molecular diagnosis of a wide variety of orodental diseases. Furthermore, our panel will contribute to better understanding the contribution of these genes to orodental disease. Trial registration numbers NCT01746121 and NCT02397824
Journal of Medical Genetics

hal-01272929
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01272929
DOI : 10.1136/jmedgenet-2015-103302
PUBMED : 26502894