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One NF1 Mutation may Conceal Another.
Pacot, Laurence; Burin des Roziers, Cyril; Laurendeau, Ingrid; Briand-Suleau, Audrey; Coustier, Audrey; Mayard, Théodora; Tlemsani, Camille; Faivre, Laurence; Thomas, Quentin; Rodriguez, Diana; Blesson, Sophie; Dollfus, Hélène; Muller, Yvon-Gauthier; Parfait, Béatrice; Vidaud, Michel; Gilbert-Dussardier, Brigitte; Yardin, Catherine; Dauriat, Benjamin; Derancourt, Christian; Vidaud, Dominique; Pasmant, Eric.
Afiliación
  • Pacot L; Service de Génétique et Biologie Moléculaires, Hôpital Cochin, HUPC, Assistance Publique-Hôpitaux de Paris, 75014 Paris, France.
  • Burin des Roziers C; Institut Cochin, INSERM U1016, Université Paris Descartes, 75014 Paris, France.
  • Laurendeau I; Service de Génétique et Biologie Moléculaires, Hôpital Cochin, HUPC, Assistance Publique-Hôpitaux de Paris, 75014 Paris, France.
  • Briand-Suleau A; Institut Cochin, INSERM U1016, Université Paris Descartes, 75014 Paris, France.
  • Coustier A; Institut Cochin, INSERM U1016, Université Paris Descartes, 75014 Paris, France.
  • Mayard T; Service de Génétique et Biologie Moléculaires, Hôpital Cochin, HUPC, Assistance Publique-Hôpitaux de Paris, 75014 Paris, France.
  • Tlemsani C; Institut Cochin, INSERM U1016, Université Paris Descartes, 75014 Paris, France.
  • Faivre L; Service de Génétique et Biologie Moléculaires, Hôpital Cochin, HUPC, Assistance Publique-Hôpitaux de Paris, 75014 Paris, France.
  • Thomas Q; Service de Génétique et Biologie Moléculaires, Hôpital Cochin, HUPC, Assistance Publique-Hôpitaux de Paris, 75014 Paris, France.
  • Rodriguez D; Service de Génétique et Biologie Moléculaires, Hôpital Cochin, HUPC, Assistance Publique-Hôpitaux de Paris, 75014 Paris, France.
  • Blesson S; Institut Cochin, INSERM U1016, Université Paris Descartes, 75014 Paris, France.
  • Dollfus H; Inserm, UMR 1231, Génétique des Anomalies du Développement, Université de Bourgogne, 21079 Dijon, France.
  • Muller YG; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Hôpital d'Enfants, 21079 Dijon, France.
  • Parfait B; Inserm, UMR 1231, Génétique des Anomalies du Développement, Université de Bourgogne, 21079 Dijon, France.
  • Vidaud M; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Hôpital d'Enfants, 21079 Dijon, France.
  • Gilbert-Dussardier B; Department of Child Neurology and National Reference Center for Neurogenetic Disorders, Armand Trousseau Hospital, GHUEP, AP-HP, INSERM U1141, 75012 Paris, France.
  • Yardin C; GRC n°19 ConCer-LD, Sorbonne Université, 75012 Paris, France.
  • Dauriat B; Service de Génétique, CHRU de Tours, 37044 Tours, France.
  • Derancourt C; Centre de référence pour les Affections Rares en Génétique Ophtalmologique (CARGO), Hôpital Civil, 67091 Strasbourg, France.
  • Vidaud D; Service de Génétique Médicale, Hôpital de Hautepierre, 67200 Strasbourg, France.
  • Pasmant E; Laboratoire de Génétique Médicale, INSERM U1112, 67000 Strasbourg, France.
Genes (Basel) ; 10(9)2019 08 22.
Article en En | MEDLINE | ID: mdl-31443423
Neurofibromatosis type 1 (NF1) is an autosomal dominant disease with complete penetrance but high variable expressivity. NF1 is caused by loss-of-function mutations in the NF1 gene, a negative regulator of the RAS-MAPK pathway. The NF1 gene has one of the highest mutation rates in human disorders, which may explain the outbreak of independent de novo variants in the same family. Here, we report the co-occurrence of pathogenic variants in the NF1 and SPRED1 genes in six families with NF1 and Legius syndrome, using next-generation sequencing. In five of these families, we observed the co-occurrence of two independent NF1 variants. All NF1 variants were classified as pathogenic, according to the American College of Medical Genetics and Genomics and the Association for Molecular Pathology (ACMG-AMP) guidelines. In the sixth family, one sibling inherited a complete deletion of the NF1 gene from her mother and carried a variant of unknown significance in the SPRED1 gene. This variant was also present in her brother, who was diagnosed with Legius syndrome, a differential diagnosis of NF1. This work illustrates the complexity of molecular diagnosis in a not-so-rare genetic disease.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Neurofibromatosis 1 / Manchas Café con Leche / Neurofibromina 1 / Proteínas Adaptadoras Transductoras de Señales Tipo de estudio: Guideline Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Genes (Basel) Año: 2019 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Neurofibromatosis 1 / Manchas Café con Leche / Neurofibromina 1 / Proteínas Adaptadoras Transductoras de Señales Tipo de estudio: Guideline Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Genes (Basel) Año: 2019 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Suiza