Sakoda K, Ishikawa S, Uozumi T, Hirakawa K, Okazaki H, Harada Y
J Neurosurg. 1979 Sep;51(3):397-401. doi: 10.3171/jns.1979.51.3.0397.
A case of sphenoethmoidal meningoencephalocele associated with agenesis of the corpus callosum and median cleft lip and palate in a baby boy is reported. Two other cases have been reported previously presenting exactly the same findings. It is possible that these malformations constitute a distinct type of congenital anomaly.
报道了一名男婴患有蝶筛部脑膜脑膨出,并伴有胼胝体发育不全及正中唇腭裂。此前曾报道过另外两例具有完全相同表现的病例。这些畸形有可能构成一种独特类型的先天性异常。