Alfieri P, Cesarini L, Zampino G, Pantaleoni F, Selicorni A, Salerni A, Vasta I, Cerutti M, Dickmann A, Colitto F, Staccioli S, Leoni C, Ricci D, Brogna C, Tartaglia M, Mercuri E
Pediatric Neurology Unit, Catholic University, Rome, Italy.
Neuropediatrics. 2008 Dec;39(6):335-40. doi: 10.1055/s-0029-1216354. Epub 2009 Jun 30.
The aim of the study was to assess various aspects of visual and visuoperceptual function in patients with Noonan syndrome (NS) or LEOPARD syndrome (LS) with mutations affecting the PTPN11, SOS1 and RAF1 genes. Twenty-four patients were assessed with a battery of tests assessing visual function including ophthalmological and orthoptic evaluation and age appropriate behavioural visual tests, including measures of crowding acuity (Cambridge crowding cards), and stereopsis (TNO test). Twenty-one subjects were also assessed with the visuo-motor integration (VMI) test. Twenty of the 24 patients (83%) had abnormalities of visual function on at least one of the tests used to assess visual function or on ophthalmological examination, and 7 of 21 (33%) also had abnormalities on VMI. Ocular movements and stereopsis were most frequently abnormal (50% and 79%, respectively). Our results suggest that visual and visuoperceptual abilities are commonly impaired in patients with Noonan and LEOPARD syndrome and they are probably related to a multifactorial etiology.
本研究的目的是评估患有努南综合征(NS)或豹皮综合征(LS)且PTPN11、SOS1和RAF1基因发生突变的患者视觉和视觉感知功能的各个方面。对24名患者进行了一系列评估视觉功能的测试,包括眼科和斜视矫正评估以及适合其年龄的行为视觉测试,包括拥挤视力测量(剑桥拥挤卡片)和立体视觉测量(TNO测试)。还对21名受试者进行了视觉运动整合(VMI)测试。24名患者中有20名(83%)在用于评估视觉功能的至少一项测试或眼科检查中存在视觉功能异常,21名患者中有7名(33%)在VMI测试中也存在异常。眼球运动和立体视觉异常最为常见(分别为50%和79%)。我们的研究结果表明,努南综合征和豹皮综合征患者的视觉和视觉感知能力通常受损,且可能与多因素病因有关。