16 results on '"D. Forgues"'
Search Results
2. Cost Production and Utilization in Collaborative Delivery Methods in the Construction Industry
- Author
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P. Martel, D. Forgues, and C. Boton
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- 2022
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3. A Framework Supporting the Empirical Evaluation of BIM Assessment Models
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E. Nonirit, D. Forgues, and É. Poirier
- Published
- 2022
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4. From Collaborative BIM to Value-Driven Asset Management: A Case Study
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D. Forgues, A. Motamedi, and M. Boize
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- 2022
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5. Diagnostic échographique d’une invagination intestinale aiguë chez l’enfant et impact thérapeutique
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D. Forgues, N. Sevette-Bechard, C. Baud, J. Eulliot, S. David, I. Taleb-Arrada, O. Prodhomme, J. Bolivar-Perrin, and M. Saguintaah
- Abstract
Resume L’invagination intestinale aigue (IIA) est l’urgence abdominale la plus frequente du jeune enfant. La penetration d’un segment intestinal dans l’intestin d’aval entraine une obstruction digestive et une compression vasculaire au niveau du collet. L’echographie est l’examen diagnostique. Elle detecte une masse digestive de 20–45 mm de diametre anteroposterieur en « cocarde » ou en « cible » centree par le segment invagine et son meso. Elle permet de determiner le type anatomique du boudin, d’identifier une souffrance digestive, de depister une lesion primitive, et donc de guider la prise en charge therapeutique. La forme ileocolique « idiopathique » (80 % des cas) due a une hyperplasie lymphoide du carrefour ileocaecal, est habituellement reduite par lavement ou insufflation gazeuse. La forme ileoileocolique (10 % des cas) est reperee en cas de souffrance digestive grâce a l’association des deux criteres de gravite : l’occlusion du grele et le liquide piege a la tete du boudin. L’IIA grelo-grelique occlusive (8 % des cas) survient sur un terrain particulier et/ou sur une lesion primitive. Le traitement est chirurgical excepte en cas de lymphome de Burkitt dissemine prouve histologiquement. L’IIA colocolique (2 % des cas) non occlusive facilement reduite par le lavement, recidive en l’absence d’exerese de la cause.
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- 2019
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6. Exploring the synergies between Life Cycle cost / Whole Life Cost and Building Information Modeling: A Systematic Literature Review
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A Yousfi, E A Poirier, and D Forgues
- Subjects
General Medicine ,General Chemistry - Abstract
Life Cycle Costing (LCC) is a cost estimating approach for project and asset planning and delivery that considers the direct and indirect costs incurred over the entire life cycle of an asset. This approach can be expanded to the concept of Whole Life Cost (WLC), which additionally considers externalities and benefits. WLC can demonstrate the financial impacts, both positive and negative, of a project on its environment, in other words it can show its complete value. Despite its potential, the approach is still perceived as complex because, among other things, access to data can be difficult and the approach is still not supported by a standardized methodology. Building Information Modeling (BIM) could be used to address these issues as both WLC and BIM are deemed complementary. BIM provides WLC with better data management, improved calculation accuracy and visualization of project impacts. In return, WLC improves project understanding, decision making and reinforces life cycle thinking. This paper aims to study the potential synergies between BIM and WLC through a systematic literature review. The identification of these synergies helped form a frame of reference to better understand the opportunities that this combination can offer. Future studies would be needed to explore the application of BIM and WLC at different project scales and identify the context in which the combination of BIM and WLC is the most beneficial.
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- 2022
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7. Phenotypic switch of smooth muscle cells in paediatric chronic intestinal pseudo‐obstruction syndrome
- Author
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Annick Bourret, Delphine Martire, Christophe Chardot, John Rendu, Marc Bellaiche, Sarah Garnier, Dominique Berrebi, Pascal de Santa Barbara, Sébastien Sagnol, Sandrine Faure, Stéphane Marchal, Nicolas Kalfa, D. Forgues, Amandine Guérin, Norbert Chauvet, Physiologie & médecine expérimentale du Cœur et des Muscles [U 1046] (PhyMedExp), and Université de Montpellier (UM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
- Subjects
0301 basic medicine ,Intestinal pseudo-obstruction ,Male ,Adolescent ,medicine.medical_treatment ,[SDV]Life Sciences [q-bio] ,Myocytes, Smooth Muscle ,chronic intestinal pseudo‐obstruction Disease ,PDGFR pathway ,PDGFRA ,Biology ,03 medical and health sciences ,0302 clinical medicine ,medicine ,Myocyte ,Humans ,Progenitor cell ,Child ,Cells, Cultured ,ComputingMilieux_MISCELLANEOUS ,Cell Proliferation ,Phenotypic plasticity ,Growth factor ,Mesenchymal stem cell ,Intestinal Pseudo-Obstruction ,Cell Differentiation ,Cell Biology ,Original Articles ,medicine.disease ,musculoskeletal system ,Phenotype ,Cell biology ,smooth muscle cells ,030104 developmental biology ,030220 oncology & carcinogenesis ,plasticity ,cardiovascular system ,Molecular Medicine ,Original Article ,Female ,tissues ,intestinal motility disorders ,Muscle Contraction ,Signal Transduction - Abstract
Smooth Muscle Cells (SMC) are unique amongst all muscle cells in their capacity to modulate their phenotype. Indeed, SMCs do not terminally differentiate but instead harbour a remarkable capacity to dedifferentiate, switching between a quiescent contractile state and a highly proliferative and migratory phenotype, a quality often associated to SMC dysfunction. However, phenotypic plasticity remains poorly examined in the field of gastroenterology in particular in pathologies in which gut motor activity is impaired. Here, we assessed SMC status in biopsies of infants with chronic intestinal pseudo‐obstruction (CIPO) syndrome, a life‐threatening intestinal motility disorder. We showed that CIPO‐SMCs harbour a decreased level of contractile markers. This phenotype is accompanied by an increase in Platelet‐Derived Growth Factor Receptor‐alpha (PDGFRA) expression. We showed that this modulation occurs without origin‐related differences in CIPO circular and longitudinal‐derived SMCs. As we characterized PDGFRA as a marker of digestive mesenchymal progenitors during embryogenesis, our results suggest a phenotypic switch of the CIPO‐SMC towards an undifferentiated stage. The development of CIPO‐SMC culture and the characterization of SMC phenotypic switch should enable us to design therapeutic approaches to promote SMC differentiation in CIPO.
- Published
- 2021
- Full Text
- View/download PDF
8. Prenatal and postnatal evolution of isolated fetal splenic cysts
- Author
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D. Forgues, Jean-Michel Faure, Anaïg Flandrin, Florent Fuchs, Camille Sauvageot, Olivier Prodhomme, and E Mousty
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Adult ,medicine.medical_specialty ,Splenic cyst ,Prenatal diagnosis ,Ultrasonography, Prenatal ,Young Adult ,03 medical and health sciences ,0302 clinical medicine ,Pregnancy ,030225 pediatrics ,parasitic diseases ,Prevalence ,medicine ,Humans ,Cyst ,Young adult ,Genetics (clinical) ,Retrospective Studies ,Splenic Diseases ,Fetus ,030219 obstetrics & reproductive medicine ,Cysts ,Obstetrics ,business.industry ,Obstetrics and Gynecology ,Gestational age ,medicine.disease ,Fetal Diseases ,Female ,France ,Splenic disease ,business - Abstract
Objectives The aim of this study was to evaluate the prevalence, the prenatal, and postnatal evolution of isolated fetal splenic cysts. Methods All cases of suspected fetal splenic cyst or abdominal unidentified cyst discovered during routine ultrasound scan, from 2007 to 2017, and referred to a French tertiary care center, were retrospectively collected. For each case, several prenatal parameters and postnatal evolution were reported. Results Among 5450 cases of fetal anomalies, 14 patients (0.3%) had a prenatal diagnosis of fetal splenic cysts. Median gestational age at diagnosis was 30.1 weeks. A unique cyst was present in 78.6%, whereas 2 cysts were observed in 14.3% and 3 cysts in 7.1%. During the pregnancy, cysts remained the same (78.6%) or disappeared (21.4%). Ultrasound scans at 6 months of age found total disappearance of the cysts (36.4%), spontaneous reduction from 2 to 1 cyst (18.2%) or persistence of the cysts (45.4%). Conclusion Fetal splenic cysts are rare images, always isolated, usually unique and mainly found during third trimester of pregnancy. Their evolution is to disappear spontaneously during pregnancy or at 6 months of age leaving only half of them to remain beyond that age but without any symptoms.
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- 2018
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9. Assessment of existing BIM implementation processes of a public organization to improve building assets management and maintenance
- Author
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N Boufares, A Motamedi, I Iordanova, and D Forgues
- Abstract
In the lifecycle of a building, the longest phase is generally that of operation and maintenance (O&M). The data needed to support O&M is mainly generated during the design, construction, and commissioning of the built asset phases. However, the extraction and transfer of relevant O&M data from the project documents remain a major issue in that it is time consuming and error prone. Nowadays, Building Information Modeling (BIM) allows different project team members to collaborate and share building data in real time. However, as-built models handed-over to the asset management team are quite voluminous and usually lack the necessary information for the O&M phase. This is due to an absence of O&M information requirements specification, and the lack of compliance monitoring and control during the project. This paper presents an action research focused on the issues encountered by a public building owner to manage their BIM processes. It demonstrates issues of BIM readiness and capabilities, both at the project and O&M levels, by mapping the gaps in the existing processes. Building owners rely on the design professionals’ expertise to guide them but do not have the adequate resources, knowledge, and tools to ensure the quality of the models delivered regarding O&M requirements. Major issues in the management of information for O&M were identified, and some recommendations are proposed.
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- 2022
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10. BIM and Lean for value generation in the built asset industry: an information management perspective
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D Mehran, E A Poirier, and D Forgues
- Abstract
The built asset industry’s notorious productivity gap is being targeted through digitalization, operationalized through Building Information Modelling (BIM), and the application of Lean philosophy to the planning, design, delivery, maintenance, and management of the built environment. While both approaches grow in popularity, their development has remained largely on parallel tracks. Both approaches have existed, for the most part, as two independent initiatives aimed at improving performance and productivity. An increasing amount of work however is pointing to the significant potential that can be achieved through the integration of both approaches. This paper investigates the mutual relations and synergies between BIM and Lean from an information management perspective. The paper also presents the key similarities, differences, synergies, and interactions between these two main drivers of built asset industry reform, while providing an investigation into the principles guiding the application of both within the construction industry.
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- 2022
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11. MP64-17 INCIDENCE OF FEBRILE URINARY TRACT INFECTION IN CHILDREN WITH HIRSCHSPRUNG DISEASE IS INCREASED IN THE FIRST MONTHS OF LIFE
- Author
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Claude Borrione, D. Forgues, Thierry Merrot, C. Lopez, Nicolas Kalfa, H. Allal, Faten Letaief, Benoit Tessier, Jean-Michel Guys, Anne Dariel, Olivier Maillet, Sarah Garnier, and M. P. Guibal
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Pediatrics ,medicine.medical_specialty ,business.industry ,Febrile urinary tract infection ,Urology ,Incidence (epidemiology) ,Medicine ,Disease ,business - Published
- 2019
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12. Prenatal diagnosis of antenatal midgut volvulus: Specific ultrasound features
- Author
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Frédéric Grosjean, Jean-Michel Faure, Caroline Bartholmot, Florent Fuchs, D. Forgues, Olivier Prodhomme, Alain Couture, Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Centre Hospitalier Universitaire de Nîmes (CHU Nîmes), Centre de recherche en épidémiologie et santé des populations (CESP), and Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris-Sud - Paris 11 (UP11)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)
- Subjects
medicine.medical_specialty ,Perinatal Death ,Gestational Age ,Prenatal diagnosis ,Autopsy ,Ultrasonography, Prenatal ,03 medical and health sciences ,0302 clinical medicine ,Pregnancy ,Prenatal Diagnosis ,parasitic diseases ,Humans ,Medicine ,Fetal Movement ,Genetics (clinical) ,Retrospective Studies ,030219 obstetrics & reproductive medicine ,business.industry ,Obstetrics ,Infant, Newborn ,Pregnancy Outcome ,Obstetrics and Gynecology ,Gestational age ,Prognosis ,medicine.disease ,3. Good health ,Volvulus ,Intestinal malrotation ,030220 oncology & carcinogenesis ,Atresia ,Fetal movement ,Premature Birth ,Female ,business ,Digestive System Abnormalities ,[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology ,Intestinal Volvulus - Abstract
International audience; OBJECTIVE:To assess specific, direct, and indirect prenatal ultrasound features in cases of fetal midgut volvulus.METHODS:Retrospective case series of neonatal volvulus, based on postnatal and prenatal imaging findings that occurred from 2006-2017. Prenatal and postnatal signs including the specific "whirlpool sign" were computed. Postnatal volvulus was confirmed by pathology examination after surgery or neonatal autopsy.RESULTS:Thirteen cases of midgut volvulus were identified. Though not a specific sign, a decrease in active fetal movements was reported in eight patients (61.5%). The prenatal whirlpool sign was directly seen in 10 cases, while an indirect but suggestive sign, a fluid-filled level within the dilated loops, was present in five cases. No intestinal malrotation was observed. Pregnancy outcomes were two terminations of pregnancy, both associated with cystic fibrosis, one early neonatal death, three prenatal spontaneous regressions, and seven favorable outcomes after neonatal surgery with resection of midgut atresia.CONCLUSIONS:Identification of the whirlpool sign or of a fluid-filled level within the dilated loops improves the accuracy of ultrasound findings for suspected volvulus. In the absence of total volvulus (in cases of intestinal malrotation) or association with cystic fibrosis, the prognosis appears good.
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- 2018
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13. Performance of Prenatal Ultrasound Screening for the Relative Positioning of Mesenteric Vessels.
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Faure JM, Larroque-Devigne A, Forgues D, Mousty E, Couture A, Kalfa N, Prodhomme O, and Fuchs F
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- Humans, Female, Pregnancy, Prospective Studies, Mesenteric Veins diagnostic imaging, Mesenteric Veins embryology, Cohort Studies, Adult, Reproducibility of Results, Ultrasonography, Prenatal methods, Mesenteric Artery, Superior diagnostic imaging, Mesenteric Artery, Superior embryology
- Abstract
Objectives: Abnormal relative positioning of the superior mesenteric artery (SMA) and vein (SMV) can lead to intestinal malrotation that predisposes to midgut volvulus. The aim of this study was to assess the prenatal ultrasound ability to visualize the relative position of SMA and SMV in normal pregnancies., Methods: Prospective cohort study performed in Montpellier University Hospital Centre, including 80 fetuses during routine 3rd trimester ultrasound scan. For each fetus included, the relative position of the vessels on an axial image was defined as SMV on the right, forward, or on the left of SMA. Doppler imaging was additionally used if necessary. Data were compared to the neonatal abdominal scans performed by pediatric radiologist., Results: The superior mesenteric vessels were identified in 79 fetuses. Prenatal findings showed a usual relative position of the vessels, that is, the vein on the right of the artery, in 96.2%. In 2 cases, the vein was strictly in front of the artery, and in 1 case, the vein was on the left side of the artery. Seventy-four neonates were examined and comparison with prenatal finding showed a perfect agreement (Kappa coefficient of 100%). An intestinal malrotation was postnatally diagnosed corresponding to the case where vein was on the left side of the artery., Conclusion: This study showed that the relative position of the SMA and SMV could be assessed using ultrasound prenatal examination with a perfect agreement with postnatal findings. In case of abnormal vessels positioning more examinations should be promote including prenatal MRI and postnatal conventional radiologic examinations to confirm intestinal malrotation., (© 2024 The Author(s). Journal of Ultrasound in Medicine published by Wiley Periodicals LLC on behalf of American Institute of Ultrasound in Medicine.)
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- 2025
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14. Anti-reflux surgery in children with congenital diaphragmatic hernia: A prospective cohort study on a controversial practice.
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Montalva L, Carricaburu E, Sfeir R, Fouquet V, Khen-Dunlop N, Hameury F, Panait N, Arnaud A, Lardy H, Schmitt F, Piolat C, Lavrand F, Ballouhey Q, Scalabre A, Hervieux E, Michel JL, Germouty I, Buisson P, Elbaz F, Lecompte JF, Petit T, Guinot A, Abbo O, Sapin E, Becmeur F, Forgues D, Pons M, Kamdem AF, Berte N, Auger-Hunault M, Benachi A, and Bonnard A
- Subjects
- Humans, Infant, Newborn, Child, Infant, Prospective Studies, Cohort Studies, Failure to Thrive, Fundoplication, Hernias, Diaphragmatic, Congenital complications, Hernias, Diaphragmatic, Congenital surgery
- Abstract
Introduction: Gastro-esophageal reflux disease (GERD) is the most frequent long-term morbidity of congenital diaphragmatic hernia (CDH) survivors. Performing a preventive fundoplication during CDH repair remains controversial. This study aimed to: (1) Analyze the variability in practices regarding preventive fundoplication; (2) Identify predictive factors for fundoplication. (3) Evaluate the impact of preventive fundoplication on gastro-intestinal outcomes in children with a CDH patch repair; METHODS: This prospective multi-institutional cohort study (French CDH Registry) included CDH neonates born in France between January 1st, 2010-December 31st, 2018. Patch CDH was defined as need for synthetic patch or muscle flap repair. Main outcome measures included need for curative fundoplication, tube feed supplementation, failure to thrive, and oral aversion., Results: Of 762 CDH neonates included, 81 underwent fundoplication (10.6%), either preventive or curative. Median follow-up was 3.0 years (IQR: 1.0-5.0). (1) Preventive fundoplication is considered in only 31% of centers. The rates of both curative fundoplication (9% vs 3%, p = 0.01) and overall fundoplication (20% vs 3%, p < 0.0001) are higher in centers that perform preventive fundoplication compared to those that do not. (2) Predictive factors for preventive fundoplication were: prenatal diagnosis (p = 0.006), intra-thoracic liver (p = 0.005), fetal tracheal occlusion (p = 0.002), CDH-grade C-D (p < 0.0001), patch repair (p < 0.0001). After CDH repair, 8% (n = 51) required curative fundoplication (median age: 101 days), for which a patch repair was the only independent predictive factors identified upon multivariate analysis. (3) In neonates with patch CDH, preventive fundoplication did not decrease the need for curative fundoplication (15% vs 11%, p = 0.53), and was associated with higher rates of failure to thrive (discharge: 81% vs 51%, p = 0.03; 6-months: 81% vs 45%, p = 0.008), tube feeds (6-months: 50% vs 21%, p = 0.02; 2-years: 65% vs 26%, p = 0.004), and oral aversion (6-months: 67% vs 37%, p = 0.02; 1-year: 71% vs 40%, p = 0.03)., Conclusions: Children undergoing a CDH patch repair are at high risk of requiring a curative fundoplication. However, preventive fundoplication during a patch repair does not decrease the need for curative fundoplication and is associated with worse gastro-intestinal outcomes in children., Level of Evidence: II - Prospective Study., Competing Interests: Declaration of Competing Interest The authors have no conflicts of interest relevant to this article to disclose., (Copyright © 2022. Published by Elsevier Inc.)
- Published
- 2022
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15. Phenotypic switch of smooth muscle cells in paediatric chronic intestinal pseudo-obstruction syndrome.
- Author
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Martire D, Garnier S, Sagnol S, Bourret A, Marchal S, Chauvet N, Guérin A, Forgues D, Berrebi D, Chardot C, Bellaiche M, Rendu J, Kalfa N, Faure S, and de Santa Barbara P
- Subjects
- Adolescent, Cell Proliferation, Cells, Cultured, Child, Female, Humans, Intestinal Pseudo-Obstruction metabolism, Male, Myocytes, Smooth Muscle metabolism, Signal Transduction, Cell Differentiation, Intestinal Pseudo-Obstruction pathology, Muscle Contraction, Myocytes, Smooth Muscle pathology, Phenotype
- Abstract
Smooth Muscle Cells (SMC) are unique amongst all muscle cells in their capacity to modulate their phenotype. Indeed, SMCs do not terminally differentiate but instead harbour a remarkable capacity to dedifferentiate, switching between a quiescent contractile state and a highly proliferative and migratory phenotype, a quality often associated to SMC dysfunction. However, phenotypic plasticity remains poorly examined in the field of gastroenterology in particular in pathologies in which gut motor activity is impaired. Here, we assessed SMC status in biopsies of infants with chronic intestinal pseudo-obstruction (CIPO) syndrome, a life-threatening intestinal motility disorder. We showed that CIPO-SMCs harbour a decreased level of contractile markers. This phenotype is accompanied by an increase in Platelet-Derived Growth Factor Receptor-alpha (PDGFRA) expression. We showed that this modulation occurs without origin-related differences in CIPO circular and longitudinal-derived SMCs. As we characterized PDGFRA as a marker of digestive mesenchymal progenitors during embryogenesis, our results suggest a phenotypic switch of the CIPO-SMC towards an undifferentiated stage. The development of CIPO-SMC culture and the characterization of SMC phenotypic switch should enable us to design therapeutic approaches to promote SMC differentiation in CIPO., (© 2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.)
- Published
- 2021
- Full Text
- View/download PDF
16. Prenatal imaging of genital defects: clinical spectrum and predictive factors for severe forms.
- Author
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Fuchs F, Borrego P, Amouroux C, Antoine B, Ollivier M, Faure JM, Lopez C, Forgues D, Faure A, Merrot T, Boulot P, Jeandel C, Philibert P, Gaspari L, Sultan C, Paris F, and Kalfa N
- Subjects
- Female, Fetus diagnostic imaging, Humans, Male, Penis abnormalities, Penis diagnostic imaging, Penis pathology, Pregnancy, Retrospective Studies, Genital Diseases, Male congenital, Genital Diseases, Male diagnostic imaging, Genital Diseases, Male pathology, Ultrasonography, Prenatal
- Abstract
Objectives: To report the clinical spectrum of genital defects diagnosed before birth, identify predictive factors for severe phenotypes at birth, and determine the rate of associated malformations., Patients and Methods: A retrospective study (2008-2017) of 4580 fetuses, identified prenatally with abnormalities evaluated by our Reference Center for Fetal Medicine, included cases with fetal sonographic findings of abnormal genitalia or uncertainty of fetal sex determination. Familial, prenatal and postnatal data were collected via a standardised questionnaire., Results: In all, 61 fetuses were included. The positive predictive value (PPV) of the prenatal diagnosis of genital defects was 90.1%. Most cases were 46,XY-undervirilized boys, 42 cases (68.8%), which included 29 with mid-penile or posterior hypospadias, nine with anterior hypospadias, and epispadias, micropenis, scrotal transposition, and buried penis (one each). In all, 46,XX-virilized girls were identified in seven cases (11.5%), which included four with congenital adrenal hyperplasia, two with isolated clitoromegaly, and one with ovotestis. Other defects included prune belly syndrome and persistent cloaca (six cases). Early detection during the second trimester (58.1% vs 18.8%, P = 0.03), intra-uterine growth restriction (IUGR) (45.2% vs 9.1%, P = 0.06), and curvature of the penis (38.7% vs 0%, P = 0.02), were more frequently related to severe defects in male newborns. Associated malformations (14 cases, 22.9%) and genetic defects (six) were frequent in undervirilized boys., Conclusion: Prenatal imaging of genital defects leads to a wide range of phenotypes at birth. Its PPV is high and extra-urinary malformations are frequent. Early diagnosis during the second trimester, associated IUGR, and curvature of the genital tubercle, should raise suspicion of a severe phenotype and may justify delivery near a multidisciplinary disorders/differences of sex development team., (© 2019 The Authors BJU International © 2019 BJU International Published by John Wiley & Sons Ltd.)
- Published
- 2019
- Full Text
- View/download PDF
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