Ocular Suppression Development at Age 12 Years

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Abstract

BACKGROUND: The patient experienced idiopathic increased intracranial pressure (pseudotumor cerebri syndrome) leading to an acquired, constant left exotropia at age 12 years. She had diplopia for about 2 months which resolved due to apparent suppression of the left eye. The patient has maintained the suppression without developing amblyopia through her current age of 17 years despite a stable large left exotropia, optic atrophy, and visual field defect. SIGNIFICANCE: The case is unusual because suppression has been assumed to develop only prior to age 10 years. BACKGROUND AND PURPOSE: Ocular suppression is an active neuroplastic process and is presumably limited to a sensitive period in childhood. It occurs when there is a difference in image clarity between the two eyes. The two most common causes are clinically significant anisometropia and strabismus. The strabismus may be monocular and constant, alternating and constant, or intermittent. The presence of suppression in anisometropia or constant monocular strabismus often leads to monocular amblyopia. The literature contains extensive animal, laboratory, and clinical evidence on the sensitive period of amblyopia, its causes, and its remediation. It is well established that amblyopia develops prior to about age 7 years, can recur up to about age 10 years, but does not develop, recur, or regress after age 12 years. Generally, response to amblyopia treatment is most robust during the sensitive period, but it is well documented that successful treatment is possible through the teen years and even adulthood. Few reports exist on suppression without amblyopia and most are based on clinical experience. von Noorden and Campos state: “As with other sensorial adaptations, such as amblyopia and anomalous retinal correspondence (ARC), the ability to suppress is limited to the immature visual system, that is, it develops only in children. Although no comparative studies exist, it is our clinical impression that the sensitive period during which suppression may develop ends after the age of 8 or 9 years”. The present paper reports an interesting case of an apparent onset of suppression at age 12 years in a patient with acquired, constant, unilateral strabismus secondary to idiopathic increased intracranial pressure.
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12岁儿童眼抑制发育
背景:该患者在12岁时经历了特发性颅内压增高(假性脑瘤综合征),导致获得性、持续性左外斜视。她患有复视约2个月,由于左眼明显抑制而消退。尽管患者有稳定的左外斜视、视神经萎缩和视野缺损,但患者在目前的17岁期间一直保持抑制作用,未发生弱视。意义:该病例是不寻常的,因为抑制被认为只在10岁之前发展。背景与目的:眼抑制是一种活跃的神经可塑性过程,可能仅限于儿童时期的敏感期。当两只眼睛之间的图像清晰度存在差异时,就会发生这种情况。两种最常见的原因是临床上显著的屈光参差和斜视。斜视可以是单眼持续性斜视、交替性斜视或间歇性斜视。在屈光参差或持续性单眼斜视中存在抑制常导致单眼弱视。文献包含广泛的动物,实验室和临床证据的敏感期弱视,其原因,及其补救措施。众所周知,弱视在7岁以前就开始发展,10岁以前可以复发,但12岁以后不会发展、复发或退化。一般来说,对弱视治疗的反应在敏感期是最强劲的,但有充分的证据表明,成功的治疗可能贯穿青少年甚至成年期。目前关于抑制无弱视的报道很少,大多数是基于临床经验。von Noorden和Campos指出:“与其他感官适应一样,如弱视和视网膜异常对应(ARC),抑制能力仅限于未成熟的视觉系统,也就是说,它只在儿童中发展。虽然没有比较研究存在,但我们的临床印象是,抑制可能发展的敏感期在8岁或9岁后结束。本文报告了一个有趣的病例,在12岁时,患者获得性,持续性,单侧斜视继发于特发性颅内压升高。
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