Abid F, Hall R, Hudgson P, Weiser R
J Neurol Sci. 1978 Feb;35(2-3):309-15. doi: 10.1016/0022-510x(78)90011-4.
The association of congenital ophthalmoplegia and facial paresis (Moebius syndrome) with a variety of other developmental somatic defects has been widely recognised. Its co-existence with hypogonadism of hypothalamic/pituitary origin and subclinical peripheral neuropathy has been reported and in this paper we describe the second case of the Moebius syndrome in association with hypogonadotrophic hypogonadism and a progressive peripheral neuropathy of mixed axonal and demyelinating type.
先天性眼肌麻痹与面瘫（默比厄斯综合征）与多种其他发育性躯体缺陷的关联已得到广泛认可。其与下丘脑/垂体起源的性腺功能减退和亚临床周围神经病变并存的情况已有报道，在本文中，我们描述了默比厄斯综合征合并低促性腺激素性性腺功能减退以及轴索性和脱髓鞘性混合型进行性周围神经病变的第二例病例。
