Congenital unilateral facial palsy revealing a facial nerve agenesis: a case report and review of the literature

被引：3

作者：

Elikplim Nordjoe, Yaotse ^{[1
]}

Azdad, Ouidad ^{[1
]}

Lahkim, Mohamed ^{[1
]}

Jroundi, Laila ^{[1
]}

Zahrae Laamrani, Fatima ^{[1
]}

机构：

[1] Ibn Sina Hosp, Dept Imaging, Rabat, Morocco

来源：

BJR CASE REPORTS | 2019年 / 5卷 / 01期

关键词：

D O I：

10.1259/bjrcr.20180029

中图分类号：

R8 [特种医学]; R445 [影像诊断学];

学科分类号：

1002 ; 100207 ; 1009 ;

摘要：

Facial nerve aplasia is an extremely rare condition that is usually syndromic, namely, in Moebius syndrome. The occurrence of isolated agenesis of facial nerve is even rarer, with only few cases reported in the literature. We report a case of congenital facial paralysis due to facial nerve aplasia diagnosed on MRI, while no noticeable abnormality was detected on the temporal bone CT.

引用

页数：3

共 10 条

[1] Congenital bilateral facial nerve hypoplasia with sensorineural hearing loss: A case report [J].