Khan Arif O, Almutlaq Mohammed, Oystreck Darren T, Engle Elizabeth C, Abu-Amero Khaled, Bosley Thomas
a Division of Pediatric Ophthalmology , King Khaled Eye Specialist Hospital , Riyadh , Saudi Arabia .
b Department of Ophthalmology , College of Medicine, King Saud University , Riyadh , Saudi Arabia .
Ophthalmic Genet. 2016 Jun;37(2):130-6. doi: 10.3109/13816810.2014.926942. Epub 2014 Jun 18.
Congenital fibrosis of the extraocular muscles type 2 (CFEOM2) is a distinct non-syndromic form of congenital incomitant strabismus secondary to orbital dysinnervation from recessive mutations in the gene PHOX2A. The phenotype includes bilateral ptosis, very large angle exotropia, ophthalmoplegia, and poorly-reactive pupils. Other than amblyopia, afferent visual dysfunction has not been considered part of CFEOM2; however, we have repeatedly observed non-amblyopic subnormal vision in affected patients. The purpose of this study was to document this recurrent feature of the phenotype.
A retrospective case series (2002-2012).
Eighteen patients (four families) were identified; all affected individuals had confirmed homozygous recessive PHOX2A mutations except one individual for whom genetic testing was not done because of multiple genetically confirmed family members. Age at assessment ranged from 5-62 years old (median 10 years old). All patients had decreased best-corrected visual acuity not completely explainable by amblyopia in both the preferred and non-preferred eye. In those patients who had further ancillary testing, visual fields (five patients) and electroretinography (10 patients) confirmed abnormalities not ascribable to amblyopia.
In addition to a distinct form of congenital incomitant strabismus, the phenotype of CFEOM2 includes subnormal vision consistent with retinal dysfunction. This could be the direct result of PHOX2A mutations or a secondary effect of orbital dysinnervation.
先天性眼外肌纤维化2型(CFEOM2)是一种独特的非综合征型先天性非共同性斜视,继发于PHOX2A基因隐性突变导致的眼眶神经支配异常。其表型包括双侧上睑下垂、大角度外斜视、眼肌麻痹和瞳孔反应不良。除弱视外,传入性视觉功能障碍未被视为CFEOM2的一部分;然而,我们在受影响的患者中反复观察到非弱视性视力低下。本研究的目的是记录这一反复出现的表型特征。
一项回顾性病例系列研究(2002 - 2012年)。
共确定了18例患者(4个家系);除1例因多名家庭成员基因检测已确诊而未进行基因检测的个体外,所有受影响个体均确诊为纯合隐性PHOX2A突变。评估时的年龄范围为5 - 62岁(中位数10岁)。所有患者的最佳矫正视力均下降,优势眼和非优势眼的视力下降不能完全用弱视来解释。在那些进行了进一步辅助检查的患者中,视野检查(5例患者)和视网膜电图检查(10例患者)证实了异常,这些异常不能归因于弱视。
除了一种独特的先天性非共同性斜视形式外,CFEOM2的表型还包括与视网膜功能障碍一致的视力低下。这可能是PHOX2A突变的直接结果或眼眶神经支配异常的继发效应。