Binder's syndrome: a phenotype rather than a definitive diagnosis?

Eleonora Mazzone, Teresa Cos Sanchez, Nicola Persico, Mieke M Cannie, Jacques Jani

Research output: Contribution to journalArticle

1 Citation (Scopus)


Binder's Syndrome is a congenital malformation characterized by nasomaxillary hypoplasia. It can be isolated or associated with multiple aetiologies, such as maternal intake of coumarin-based anticoagulants during pregnancy, systemic lupus erythematosus and some other monogenic conditions, such as Keutel syndrome or Chondrodysplasia punctata (CDP). [1] This article is protected by copyright. All rights reserved.

Original languageEnglish
Pages (from-to)131-132
Number of pages2
JournalUltrasound in Obstetrics and Gynecology
Issue number1
Publication statusPublished - Jan 2019


  • Binder Syndrome
  • Chondrodysplasia Punctata
  • Prenatal diagnosis
  • Ultrasound


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