Verzijl Harriëtte T F M, Valk Jaap, de Vries Rob, Padberg George W
Department of Neurology, University Medical Center Nijmegen, PO Box 9101, 6500 HB Nijmegen, The Netherlands.
Neurology. 2005 Mar 8;64(5):849-55. doi: 10.1212/01.WNL.0000152980.92436.D9.
To detail the radiologic findings in Möbius syndrome, in order to clarify its pathogenetic mechanisms.
High resolution three-dimensional T1 (MP rage) and T2 (CISS) weighted MRI were used to study the cisternal and canalicular portion of the seventh cranial nerve in six Möbius patients. Also, the anteroposterior dimension of the brainstem was measured at the level of the pons in the authors' 6 patients and in 20 age-matched healthy control subjects. Furthermore, the MRIs were evaluated for associated congenital brain anomalies.
The facial nerves were absent in all six patients despite residual function in some facial muscles. The authors confirmed brainstem hypoplasia but did not find tegmental calcifications. The anteroposterior dimension of the brainstem ranged between 17 and 25 mm vs 20 to 27 mm for controls. In three patients there were congenital abnormalities in the posterior fossa.
The absent facial nerves on MRI and the unusual distribution of the facial weakness, which is characteristic of Möbius syndrome, suggests that other cranial nerves, possibly the trigeminal, hypoglossal, or glossopharyngeal nerve, aberrantly innervate some lower facial muscles. Radiologic findings support the notion that Möbius syndrome is part of a more complex congenital anomaly of the fossa posterior.
详细阐述莫比乌斯综合征的影像学表现,以阐明其发病机制。
采用高分辨率三维T1(MP rage)加权和T2(CISS)加权磁共振成像,对6例莫比乌斯综合征患者的第七颅神经的脑池段和神经管段进行研究。此外,在作者的6例患者以及20例年龄匹配的健康对照者中,测量脑桥水平脑干的前后径。另外,对磁共振成像进行评估以查找相关的先天性脑异常。
所有6例患者的面神经均缺失,尽管部分面部肌肉仍有残余功能。作者证实存在脑干发育不全,但未发现被盖钙化。脑干的前后径在17至25毫米之间,而对照组为20至27毫米。3例患者存在后颅窝先天性异常。
磁共振成像显示面神经缺失以及莫比乌斯综合征特有的面部无力异常分布提示,其他颅神经,可能是三叉神经、舌下神经或舌咽神经,异常支配一些下部面部肌肉。影像学表现支持莫比乌斯综合征是后颅窝更复杂先天性异常一部分的观点。