Singh B, Shahwan S A, Singh P, al-Deeb S M, Sharif H
Department of Paediatrics, Riyadh Armed Forces Hospital, Saudi Arabia.
Acta Neurol Scand. 1992 Jun;85(6):436-8. doi: 10.1111/j.1600-0404.1992.tb06043.x.
Basal ganglia calcification has not been described in Mobius syndrome. A family with two children with Mobius syndrome are reported. Bilateral basal ganglia calcification was seen on computed tomography in both. This is the first family where cerebral involvement has been clearly documented in this syndrome.
双侧基底节钙化在先天性面瘫综合征中尚未见报道。本文报告了一个有两个患先天性面瘫综合征孩子的家庭。计算机断层扫描显示两个孩子均有双侧基底节钙化。这是首个该综合征有明确脑部受累记录的家庭。
