Literature DB >> 27162279

Prenatally Diagnosed Cases of Binder Phenotype Complicated by Respiratory Distress in the Immediate Postnatal Period.

Yair J Blumenfeld1, Alexis S Davis2, Susan R Hintz2, Kristina Milan3, Anna H Messner4, Richard A Barth5, Louanne Hudgins6, Jane Chueh3, Margaret Homeyer6, Jonathan A Bernstein7, Gregory Enns7, Paldeep Atwal7, Melanie Manning8.   

Abstract

Binder phenotype, or maxillonasal dysostosis, is a distinctive pattern of facial development characterized by a short nose with a flat nasal bridge, an acute nasolabial angle, a short columella, a convex upper lip, and class III malocclusion. We report 3 cases of prenatally diagnosed Binder phenotype associated with perinatal respiratory impairment.
© 2016 by the American Institute of Ultrasound in Medicine.

Entities:  

Keywords:  Binder phenotype; magnetic resonance imaging; obstetric ultrasound; prenatal diagnosis; respiratory distress; sonography

Mesh:

Year:  2016        PMID: 27162279     DOI: 10.7863/ultra.15.02050

Source DB:  PubMed          Journal:  J Ultrasound Med        ISSN: 0278-4297            Impact factor:   2.153


  1 in total

1.  Severe nasomaxillary hypoplasia (Binder phenotype) on prenatal US/MRI: an important marker for the prenatal diagnosis of chondrodysplasia punctata.

Authors:  Anna R Blask; Eva I Rubio; Kimberly A Chapman; Anne K Lawrence; Dorothy I Bulas
Journal:  Pediatr Radiol       Date:  2018-03-23
  1 in total

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