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Binder phenotype: clinical and etiological heterogeneity of the so-called Binder maxillonasal dysplasia in prenatally diagnosed cases,and review of the literature
Authors:J M Levaillant  D Moeglin  K Zouiten  M Bucourt  L Burglen  V Soupre  C Baumann  M L Jaquemont  R Touraine  A Picard  E Vuillard  N Belarbi  J F Oury  A Verloes  M P Vazquez  P Labrune  A L Delezoide  M Gérard-Blanluet
Institution:1. Prenatal Diagnosis Unit, APHP Antoine Béclère University Hospital, Clamart, France;2. Fetal Imaging, Grasse, France;3. Fetal Imaging, Point-à Pitre, Martinique, France;4. Fetal Pathology, APHP Jean Verdier University Hospital, Bondy, France;5. Clinical Genetics Department, APHP Armand Trousseau Hospital, France;6. Maxillo-facial Surgery, APHP Armand Trousseau University Hospital, Paris, France;7. Université Pierre et Marie Curie, Paris 6, France;8. Clinical Genetics Department, APHP Robert Debré University Hospital, Paris, France;9. Department of Genetics, Hôpital Nord, Saint Etienne, France;10. Prenatal Diagnosis, APHP Robert Debré University Hospital, Paris, France;11. Pediatric and Fetal Radiology, APHP Robert Debré University Hospital, Paris, France;12. Clinical Genetics, APHP Antoine Béclère, Université Paris Sud, UFR Kremlin-Bicêtre, Clamart, France;13. Fetal Pathology, APHP Robert Debré Hospital, Diderot University, Paris, France
Abstract:
Keywords:Binder syndrome  fetal dysmorphology  nasal bones  spina nasalis  ultrasonography  chondrodysplasia punctata
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