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- Title
Binder syndrome: a phenotype rather than a definitive diagnosis?
- Authors
Mazzone, E.; Cos Sanchez, T.; Persico, N.; Cannie, M. M.; Jani, J.; Mazzone, Eleonora; Cos Sanchez, Teresa; Persico, Nicola; Cannie, Mieke M; Jani, Jacques
- Abstract
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.
- Subjects
DIFFERENTIAL diagnosis; FETAL ultrasonic imaging; MAGNETIC resonance imaging; THIRD trimester of pregnancy; PRENATAL diagnosis; PHENOTYPES; FACIAL bone abnormalities; MULTIPLE epiphyseal dysplasia
- Publication
Ultrasound in Obstetrics & Gynecology, 2019, Vol 53, Issue 1, p131
- ISSN
0960-7692
- Publication type
case study
- DOI
10.1002/uog.19198