Engle E C, Goumnerov B C, McKeown C A, Schatz M, Johns D R, Porter J D, Beggs A H
Department of Neurology, Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Ann Neurol. 1997 Mar;41(3):314-25. doi: 10.1002/ana.410410306.
Congenital fibrosis of the extraocular muscles is an autosomal dominant congenital disorder characterized by bilateral ptosis, restrictive external ophthalmoplegia with the eyes partially or completely fixed in an infraducted (downward) and strabismic position, and markedly limited and aberrant residual eye movements. It has been generally thought that these clinical abnormalities result from myopathic fibrosis of the extraocular muscles. We describe the intracranial and orbital pathology of 1 and the muscle pathology of 2 other affected members of a family with chromosome 12-linked congenital fibrosis of the extraocular muscles. There is an absence of the superior division of the oculomotor nerve and its corresponding alpha motor neurons, and abnormalities of the levator palpebrae superioris and rectus superior (the muscles innervated by the superior division of the oculomotor nerve). In addition, increased numbers of internal nuclei and central mitochondrial clumping are found in other extraocular muscles, suggesting that the muscle pathology extends beyond the muscles innervated by the superior division of cranial nerve III. This report presents evidence that congenital fibrosis of the extraocular muscles results from an abnormality in the development of the extraocular muscle lower motor neuron system.
先天性眼外肌纤维化是一种常染色体显性先天性疾病,其特征为双侧上睑下垂、限制性眼球外肌麻痹,眼睛部分或完全固定在内转(向下)和斜视位置,以及明显受限且异常的残余眼球运动。通常认为这些临床异常是由眼外肌的肌病性纤维化引起的。我们描述了一个与12号染色体连锁的先天性眼外肌纤维化家族中1例患者的颅内和眼眶病理学情况以及另外2例受累家庭成员的肌肉病理学情况。动眼神经上支及其相应的α运动神经元缺失,提上睑肌和上直肌(由动眼神经上支支配的肌肉)存在异常。此外,在其他眼外肌中发现内核数量增加和中央线粒体聚集,这表明肌肉病理学改变超出了由动眼神经上支支配的肌肉范围。本报告提供了证据,证明先天性眼外肌纤维化是由眼外肌下运动神经元系统发育异常所致。