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Dermatological manifestations in cardiofaciocutaneous syndrome: a prospective multicentric study of 45 mutation-positive patients.
Bessis, D; Morice-Picard, F; Bourrat, E; Abadie, C; Aouinti, S; Baumann, C; Best, M; Bursztejn, A-C; Capri, Y; Chiaverini, C; Coubes, C; Giuliano, F; Hadj-Rabia, S; Jacquemont, M-L; Lacombe, D; Lyonnet, S; Mallet, S; Mazereeuw-Hautier, J; Miquel, J; Molinari, N; Parfait, B; Pernet, C; Philip, N; Pinson, L; Pouvreau, N; Vial, Y; Sarda, P; Sigaudy, S; Verloes, A; Cavé, H; Geneviève, D.
Afiliação
  • Bessis D; Department of Dermatology, Saint-Eloi Hospital, University of Montpellier, Montpellier, France.
  • Morice-Picard F; INSERM U1058, Montpellier, France.
  • Bourrat E; Department of Pediatric Dermatology, Pellegrin University Hospital of Bordeaux, Bordeaux, AP-HP, France.
  • Abadie C; Department of Pediatric Dermatology, Robert-Debré Hospital, AP-HP, Paris, France.
  • Aouinti S; Department of Clinical Genetics, Sud Hospital and University Hospital of Rennes, Rennes, France.
  • Baumann C; Department of Statistics, La Colombière Hospital and University of Montpellier, Montpellier, France.
  • Best M; Department of Clinical Genetics, Robert-Debré Hospital, AP-HP and University of Paris-Diderot, Paris, France.
  • Bursztejn AC; Department of Dermatology, Saint-Eloi Hospital, University of Montpellier, Montpellier, France.
  • Capri Y; Department of Dermatology, Brabois Hospital, University of Nancy, Nancy, France.
  • Chiaverini C; Department of Clinical Genetics, Robert-Debré Hospital, AP-HP and University of Paris-Diderot, Paris, France.
  • Coubes C; Department of Dermatology, L'Archet 2 Hospital and University of Nice, Nice, France.
  • Giuliano F; Department of Clinical Genetics, Arnaud de Villeneuve Hospital, University of Montpellier, Montpellier, France.
  • Hadj-Rabia S; Department of Clinical Genetics, L'Archet 2 Hospital and University of Nice, Nice, France.
  • Jacquemont ML; Department of Pediatric Dermatology, Necker-Enfants Malades Hospital, AP-HP, Paris, France.
  • Lacombe D; Department of Clinical Genetics, Femme-Mère-Enfant Hospital, University of South Reunion, Saint-Pierre, Réunion, France.
  • Lyonnet S; Department of Clinical Genetics, Pellegrin University Hospital of Bordeaux, Bordeaux, AP-HP, France.
  • Mallet S; Department of Clinical Genetics, Necker-Enfants Malades Hospital, AP-HP, Paris, France.
  • Mazereeuw-Hautier J; Department of Dermatology, La Timone Hospital, AP-HM and University of Marseille, Marseille, France.
  • Miquel J; Department of Dermatology, Larrey Hospital, Reference Center for Rare Skin Diseases, University of Toulouse, Toulouse, France.
  • Molinari N; Department of Pediatric Dermatology, Femme-Mère-Enfant Hospital, University of South Reunion, Saint-Pierre, Réunion, France.
  • Parfait B; Department of Dermatology, University of Rennes, Rennes, France.
  • Pernet C; Department of Statistics, La Colombière Hospital and University of Montpellier, Montpellier, France.
  • Philip N; Department of Molecular Genetics and Biology, Cochin Hospital, AP-HP, University Paris V, Paris, France.
  • Pinson L; Department of Dermatology, Saint-Eloi Hospital, University of Montpellier, Montpellier, France.
  • Pouvreau N; Department of Clinical Genetics, La Timone Hospital, AP-HM and University of Marseille, Marseille, France.
  • Vial Y; Department of Clinical Genetics, Arnaud de Villeneuve Hospital, University of Montpellier, Montpellier, France.
  • Sarda P; Department of Genetic Biochemistry, Robert-Debré Hospital, AP-HP and University of Paris-Diderot, Paris, France.
  • Sigaudy S; Department of Genetic Biochemistry, Robert-Debré Hospital, AP-HP and University of Paris-Diderot, Paris, France.
  • Verloes A; Department of Clinical Genetics, Arnaud de Villeneuve Hospital, University of Montpellier, Montpellier, France.
  • Cavé H; Department of Clinical Genetics, La Timone Hospital, AP-HM and University of Marseille, Marseille, France.
  • Geneviève D; Department of Clinical Genetics, Robert-Debré Hospital, AP-HP and University of Paris-Diderot, Paris, France.
Br J Dermatol ; 180(1): 172-180, 2019 01.
Article em En | MEDLINE | ID: mdl-30141192
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Displasia Ectodérmica / Insuficiência de Crescimento / Cardiopatias Congênitas Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Br J Dermatol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: França
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Displasia Ectodérmica / Insuficiência de Crescimento / Cardiopatias Congênitas Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Br J Dermatol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: França