Abarbanel J M, Ashby P, Marquez-Julio A, Chapman K R
Electromyography Department, Toronto Hospital, Ontario, Canada.
Can J Neurol Sci. 1991 Aug;18(3):349-51. doi: 10.1017/s0317167100031930.
A Caucasian girl developed slowly progressive sensory neural deafness and bulbar and spinal muscle weakness typical of the Vialetto-Van Laere syndrome. As the condition progressed the major disabilities became dysphagia, respiratory muscle weakness and postural hypotension. Treatment with gastrostomy feedings, oxygen and fludrocortisone acetate produced worthwhile functional improvement.
一名白种女孩出现了缓慢进展的感觉神经性耳聋以及典型的Vialetto-Van Laere综合征所具有的延髓和脊髓肌肉无力症状。随着病情进展,主要的残疾表现为吞咽困难、呼吸肌无力和体位性低血压。采用胃造口喂养、吸氧以及醋酸氟氢可的松治疗后,功能有了显著改善。