Salman Michael S, Ikeda Kristin M
Section of Pediatric Neurology (MSS), Children's Hospital and Department of Pediatrics and Child Health (MSS), Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada; and Schulich School of Medicine and Dentistry (KMI), Western University, London, Ontario, Canada.
J Neuroophthalmol. 2014 Sep;34(3):246-50. doi: 10.1097/WNO.0000000000000122.
Infantile-onset saccade initiation delay (ISID) is a defect in saccade initiation. Other features may include impaired smooth ocular pursuit, developmental delay, hypotonia, and ataxia. Brain magnetic resonance imaging (MRI) can be normal or show supratentorial or infratentorial abnormalities. Our aim was to correlate the clinical features of ISID with brain MRI findings.
Detailed review of the English medical literature between 1952 and 2012 revealed 67 studies with possible ISID. Patients without a brain MRI or with inadequate information, Joubert syndrome, neurodegenerative disorders, and acquired saccade initiation delay were excluded. Ninety-one patients (age range, 3 months to 45 years) met the inclusion criteria and were divided into 3 groups based on their brain MRI findings: normal (n = 55), supratentorial abnormalities (n = 17), and infratentorial abnormalities (n = 19). The patients' clinical features including the direction of head thrusts, smooth pursuit, optokinetic response (OKR), tone, development, and coordination were compared and analyzed among the MRI groups using χ test.
Horizontal head thrusts were significantly more common in patients with infratentorial abnormalities or normal brain MRI, whereas vertical head thrusts were more common among patients with supratentorial abnormalities (P < 0.0001). The slow phases of the OKR were significantly more likely to be impaired in patients with supratentorial or infratentorial abnormalities than in those with a normal MRI (P = 0.011). Other neuro-ophthalmological, neurological, and developmental features were similar among patients in the 3 neuroimaging groups.
The direction of head thrust and the integrity of the slow phases of the OKR are useful clinical indicators of possible sites of abnormality on brain MRI in patients with ISID.
婴儿期发作性扫视启动延迟(ISID)是一种扫视启动缺陷。其他特征可能包括平滑眼球追踪受损、发育迟缓、肌张力减退和共济失调。脑磁共振成像(MRI)可能正常,也可能显示幕上或幕下异常。我们的目的是将ISID的临床特征与脑MRI结果相关联。
对1952年至2012年间的英文医学文献进行详细回顾,发现67项可能与ISID相关的研究。排除没有脑MRI检查或信息不充分的患者、Joubert综合征、神经退行性疾病以及后天性扫视启动延迟患者。91例患者(年龄范围3个月至45岁)符合纳入标准,并根据其脑MRI结果分为3组:正常组(n = 55)、幕上异常组(n = 17)和幕下异常组(n = 19)。使用χ检验对MRI组间患者的临床特征进行比较和分析,包括头部推挤方向、平滑追踪、视动反应(OKR)、肌张力、发育和协调性。
幕下异常或脑MRI正常的患者中水平头部推挤明显更常见,而幕上异常患者中垂直头部推挤更常见(P < 0.0001)。与MRI正常的患者相比,幕上或幕下异常患者的OKR慢相明显更易受损(P = 0.011)。3个神经影像学组患者的其他神经眼科、神经学和发育特征相似。
头部推挤方向和OKR慢相的完整性是ISID患者脑MRI上可能异常部位有用的临床指标。