CPQCC Publication
| Title | Prenatally Diagnosed Cases of Binder Phenotype Complicated by Respiratory Distress in the Immediate Postnatal Period. |
| Publication Type | Journal Article |
| Year of Publication | 2016 |
| Authors | Blumenfeld YJ, Davis AS, Hintz SR, Milan K, Messner AH, Barth RA, Hudgins L, Chueh J, Homeyer M, Bernstein JA, Enns G, Atwal P, Manning M |
| Journal | J Ultrasound Med |
| Volume | 35 |
| Issue | 6 |
| Pagination | 1353-8 |
| Date Published | 2016 Jun |
| ISSN | 1550-9613 |
| Keywords | Adult, Diagnosis, Differential, Female, Humans, Infant, Newborn, Magnetic Resonance Imaging, Male, Maxillofacial Abnormalities, Pregnancy, Prenatal Diagnosis, Respiratory Insufficiency, Ultrasonography, Prenatal |
| 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. |
| DOI | 10.7863/ultra.15.02050 |
| Alternate Journal | J Ultrasound Med |
| PubMed ID | 27162279 |
