Hageman G, Willemse J, van Ketel B A, Barth P G, Lindhout D
Neuropediatrics. 1987 Feb;18(1):45-50. doi: 10.1055/s-2008-1052435.
There is evidence that the Pena-Shokeir syndrome is not a specific phenotype but should be regarded as a "fetal akinesia deformation sequence". A neuropathological study of six random new cases was performed to evaluate this theory. Brain pathology observed included persistent fetal meningeal vascularization (two cases), agenesis of the septum pellucidum (one case) and hydranencephaly (one case). Investigation of the spinal cord (in two cases) revealed no abnormalities. Muscle histology (in four cases) was indicative of neurogenic atrophy in two cases. These findings are compared with the data of the 28 cases previously described. It is concluded that the Pena-Shokeir syndrome is a heterogeneous syndrome in which cerebral lesions may play an important role in the pathogenesis. The cerebral malformations may also indicate the time of origin and contribute in the perinatal death of this syndrome.
有证据表明,佩纳 - 绍凯尔综合征并非一种特定的表型,而应被视为一种“胎儿运动不能变形序列”。对6例随机选取的新病例进行了神经病理学研究,以评估这一理论。观察到的脑部病理学表现包括持续性胎儿脑膜血管化(2例)、透明隔缺如(1例)和积水性无脑畸形(1例)。对脊髓的检查(2例)未发现异常。肌肉组织学检查(4例)显示2例存在神经源性萎缩。将这些发现与之前描述的28例病例的数据进行了比较。得出的结论是,佩纳 - 绍凯尔综合征是一种异质性综合征,其中脑部病变可能在发病机制中起重要作用。脑部畸形也可能表明发病时间,并导致该综合征的围产期死亡。