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一个先天性眼外肌纤维化综合征家系的影像特征分析 被引量:2

Imaging features analysis of congenital fibrosis of extraocular muscles in a family
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摘要 目的:研究一个先天性眼外肌纤维化综合征(CFEOM)家系,发病者眼外肌及眼运动神经的影像学特征,初步探索该病发病机制,为其治疗提供理论基础。方法:对一个常染色体显性遗传病CFEOM1家系,三代3例患者进行高分辨率MRI扫描,随机抽取12个正常人作为对照组,扫描方法:眼眶部行3mm层厚、T1加权MRI扫描;颅内行1mm层厚、3DFIESTA扫描。比较两组眼外肌以及眼运动神经的变化。结果:发病者5条眼外肌体积较正常对照组小,尤以上直肌明显,差异有统计学意义(P<0.05);眼运动神经(动眼神经、外展神经)的颅内段截面积较正常对照组小,差异有统计学意义(P<0.05)。结论:CFEOM病患者各条眼外肌较正常人萎缩,颅内眼运动神经有发育不良。提示该病可能为眼运动神经核发育不良引起。 AIM:To study the imaging features of extraocular muscles (EOMs) and ocular motor nerves of a Chinese family with congenital fibrosis of extraocular muscles (CFEOM) by magnetic resonance imaging (MRI), and approach the etiopathogenisis of CFEOM to provide theory basis for the treatment of it.METHODS:In a autosomal dominant inheritance of CFEOM family, 2 cases of three generations were scanned by high resolution MRI, and 12 healthy people were selected as control group. Scanning method:orbital region were performed 3mm, T1-weighted imaging(T1WI); intracranial region were performed 1mm, 3D FIESTA imaging. The changes of EOMs and ocular motor nerves of two groups were compared.RESULTS:Compared to healthy people, the volumes of patients' 5 EOMs were smaller than those of control group, especially the superior rectus (P0.05) . And diameters of ocular motor nerves(oculomotor nerve, abducent nerve) were smaller, too (P0.05) .CONCLUSION:The EOMs of patients with CFEOM are atrophied compared with that of healthy people, intracranial ocular motor nerves are dysplasia, which indicates that this disease can be caused by dysplasia of ocular motor nerves.
作者 徐莹 荆小娟
出处 《国际眼科杂志》 CAS 2012年第9期1734-1738,共5页 International Eye Science
关键词 先天性眼外肌纤维化 影像学 磁共振 congenital fibrosis of extraocular muscles imaging magnetic resonance image
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参考文献11

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二级参考文献11

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共引文献18

同被引文献21

  • 1王丹,杨隆艳,宋跃.先天性广泛性眼外肌纤维化综合征[J].国际眼科杂志,2005,5(6):1243-1247. 被引量:1
  • 2赵军,赵堪兴,李宁东,焦永红,杨永佳,田裕民.先天性眼外肌纤维化伴少年白发一家系[J].中华眼科杂志,2007,43(4):319-323. 被引量:7
  • 3赵军,李宁东,赵堪兴.先天性眼外肌纤维化综合征研究进展[J].眼科研究,2007,25(7):557-560. 被引量:8
  • 4Khan AO,Khalil DS,Al Sharif LJ,et al.Germline mosaicism for KIF21A mutation(p.R954L)mimicking recessive inheritance for congenital fibrosis of the extraocular muscles.Ophthalmology 2010;117(1):154-158.
  • 5Yamada K,Hunter DG,Andrews C,et al.Anovel KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Marcus Gunn jaw-winking phenomenon.Arch Ophthalmol 2005;123(9):1254-1259.
  • 6Engle EC,Marondle I,Houtman WA,et al.congenial fibrosis of the extraocular muscles(autosomal dominant congenital external ophthalmoplegia)genetic homogeneity,linkage refinement,and physical mapping on chromosome12.Am J Hum Genet 1995;57(5):1086-1094.
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  • 8Yazdani A,Chung DC,Abbaszad eganMR,et al.A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocularmuscles type 2( CFEOM2).Am J Ophthalmol 2003;136(5):861- 865.
  • 9Doherty EJ,Macy ME,Wang SM,et al.CFEOM 3:a new extraocularcongen ital fibros is syndrome that maps to 16q24.2-q24.3.Invest Ophthalmol Vis Sci 1999;4(8):1687-1694.
  • 10Yazdani AMD,Elias I,TraboulsiM D.Classification and surgical management of patients with familialand sporadic forms of congential fibrosis of the Extraocularmuscles.Ophthalmology 2004;111(5):1035-1042.

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