NAGER ACROFACIAL DYSOSTOSIS - CASE-REPORT AND REVIEW OF THE LITERATURE

被引:22
作者
DANZIGER, I
BRODSKY, L
PERRY, R
NUSBAUM, S
BERNAT, J
ROBINSON, L
机构
[1] STATE UNIV NEW YORK BUFFALO, SCH MED & BIOMED SCI, DEPT OTOLARYNGOL, 213 BRYANT ST, BUFFALO, NY 14222 USA
[2] STATE UNIV NEW YORK BUFFALO, SCH MED & BIOMED SCI, DEPT PAEDIAT, BUFFALO, NY USA
[3] STATE UNIV NEW YORK BUFFALO, SCH MED & BIOMED SCI, DEPT SURG, BUFFALO, NY USA
[4] STATE UNIV NEW YORK BUFFALO, SCH DENT MED, DEPT PAEDIAT DENT, BUFFALO, NY USA
[5] STATE UNIV NEW YORK BUFFALO, SCH DENT MED, DEPT ORAL SURG, BUFFALO, NY USA
[6] CHILDRENS HOSP, BUFFALO, NY USA
关键词
NAGER SYNDROME; CRANIOFACIAL ANOMALY; INTERDISCIPLINARY CARE;
D O I
10.1016/0165-5876(90)90353-S
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Nager's acrofacial dysostosis is a rare congential anomaly in which mandibulofacial dysostosis is seen in combination with limb deformities, particularly hypoplasia of the radial aspect of the hand. A boy with a severe manifestation of this syndrome is presented. Deformities include severe bilateral mandibular hypoplasia with trismus, malar hypoplasia, downward sloping palpebral fissures, high-arched hard palate, absent soft palate, external auditory and middle ear abnormalities and bilateral hand deformities. The diagnosis and treatment difficulties in this patient are discussed in light of those reported in the literature. An interdisciplinary team approach to the management of patients with Nager syndrome is emphasized.
引用
收藏
页码:225 / 240
页数:16
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