Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0038379 (strabismus)
 9,317 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The clinical features of congenital nystagmus (CN) were studied statistically in 106 cases of CN. The point of the nystagmus at which the patients could best see the targets was detected in some patients. The effects of superior colliculectomy on their visual disturbance and the mechanism will be discussed. The study population comprises 106 patients, 79 males and 27 females, aged from one to 64 (mean 19.4 years). Patients with jerky type classified on ENG were found in 53 cases (50%), pendular type in 39 cases (37%), and mixed type in 14 cases (13%). Patients with jerky type showed significantly good visual acuity (mean 0.69 +/- 0.31, p less than 0.005). They showed significant abnormalities during pregnancy and delivery (p less than 0.01) and had a neutral point (p less than 0.01). Patients with pendular type, on the other hand, showed poor visual acuity (mean 0.26 +/- 0.30) and had significant frequency of family history (p less than 0.05), head tremor (p less than 0.01) and strabismus (p less than 0.01). Thirteen cases (12%) had ocular diseases which involved the retina, cornea and optic nerve. Visual function was elaborated on such parameters of ENG as perception, peak variation and plateau time. Perception, which means the ability to detect the dim flashes during the appearance of the nystagmus, was manifested by pushing a button when patients could detect flashes presented at random on the screen. At the turning point from the quick phase to the slow phase, the detection was executed most successfully. It is thought that in CN, a target is usually gazed upon at a point, changing the direction from the quick phase to the slow phase.(ABSTRACT TRUNCATED AT 250 WORDS)
No To Shinkei 1988 Sep
PMID:[A study of visual function in congenital nystagmus--mechanism of visual improvement after stereotactic superior colliculectomy]. 319 Sep 32

Iatrogenic damage to the orbital fascial system during strabismus surgery may lead to adherences with resulting problems of motility. To prevent new adherences in revisional surgery, several materials were tried, with varying degrees of success. The authors tested Polyglactin 910, popular as a suture material in strabismus surgery, in the form of a net. The material is hydrolytically soluble. Since the tissue response is finished before dissolution of the implant, it seemed that Polyglactin would be a suitable barrier to the formation of adhesions in Tenon's capsule. The implant was applied in 11 patients, some of whom had already undergone several strabismus operations and had adhesions at the surgical site. In one case the implant was used in a primary procedure. In one patient revisional surgery was needed four weeks after surgery because of overeffect, and this provided an opportunity to investigate the implanted area histologically.
Klin Monbl Augenheilkd 1988 Sep
PMID:[Polyglactin 910 implants in muscle revision surgery for the reconstruction of physiologic limits in Tenon's capsule]. 323 30

All patients exhibiting the various types of abnormal head postures of ocular origin that were seen during the last two years are presented in order to determine the relative frequency of the different causes of these postures, and the purposes they serve. The treatment modality and results are also discussed. The manuscript is divided into four parts: Part I, II, and III concern head postures in incomitant strabismus. In Part IV, head postures in Ciancia's syndrome, restrictions, and refractive errors are described.
Ann Ophthalmol 1987 Sep
PMID:Abnormal ocular head postures: Part I. 366 22

Binocular experience in infancy is necessary for the normal development of the visual cortex. However, it is not known whether binocular experience also affects the processing of specific kinds of visual information such as motion. We now report deficits in visual motion processing in 7 adult humans who lacked binocularity in infancy because of strabismus. As probes for assessing visual motion processing, we used the initiation of smooth pursuit eye movements and the judgment of target velocity independent of eye movement. Monocular viewing was essential to reveal the deficits. For horizontal pursuit, strabismic subjects showed nasal-temporal asymmetries, such that nasally directed target motion evoked more vigorous pursuit. For vertical pursuit, strabismics showed up-down asymmetries, such that upward target motion evoked more vigorous pursuit. In addition, strabismics had abnormalities in the relative effectiveness of different parts of the visual field for initiating both horizontal and vertical pursuit. Psychophysical judgements of horizontal target velocity revealed deficits analogous motion was perceived as faster than temporally directed motion, even when the 2 directions of motion were actually presented at the same speed. The magnitude of the motion processing deficits in each subject was correlated with the severity of the clinical signs of the strabismus. Our results suggest 2 possible interpretations. Maldevelopments of visual motion processing may cause strabismus in infancy, or alternatively, strabismus in the critical period for visual development may cause a maldevelopment of visual motion processing.
J Neurosci 1986 Sep
PMID:Maldevelopment of visual motion processing in humans who had strabismus with onset in infancy. 374 19

Ocular abnormalities were present in five of 11 patients with Freeman-Sheldon syndrome. The predominant ocular findings were strabismus and blepharoptosis. Stiffness of the extraocular muscles, demonstrated in three patients by forced duction testing, made surgery difficult. Two patients underwent frontalis muscle sling surgery and a third underwent levator palpebrae superioris muscle resection. Although all three remained exotropic, the cosmetic results were good.
Am J Ophthalmol 1986 Sep 15
PMID:Ocular abnormalities in the Freeman-Sheldon syndrome. 375

Three children between the ages of 4 and 6 years had untreated monocular traumatic cataracts, for several years. Although amblyopia did not develop, there was a disruption of fusion that resulted in horror fusionis after cataract surgery. Two adults with strabismus and amblyopia since childhood developed cataracts as adults. The occlusion caused by these long-standing cataracts appeared to eliminate suppression and resulted in horror fusionis.
Am J Ophthalmol 1986 Sep 15
PMID:Abnormal sensory findings secondary to monocular cataracts in children and strabismic adults. 375 1

We measured vision function in a number of 7-month-old infants with intrauterine growth retardation (IUGR) and compared these findings to those for 7-month-old infants of normal birth weight. The IUGR infants had an average visual acuity of 6/162 (20/540) and an average spherical refractive error of 1.49 D hyperopia. The normal birth weight infants had an average visual acuity of 6/118.8 (20/396) and an average spherical refractive error of 0.94 D hyperopia. However, the differences between the infant groups for visual acuity and refractive error were not statistically significant. Anisometropia, astigmatism, and strabismus were infrequent for both infant groups. The results of this study suggest that IUGR infants have visual abilities resembling those of normal birth weight infants.
Am J Optom Physiol Opt 1986 Sep
PMID:Clinical comparison of the visual parameters in infants with intrauterine growth retardation vs. infants with normal birth weight. 377 18

A 36-year-old male had been constantly wearing a patch to avoid diplopia since an operation on the right parietal area of the brain. Postsurgical visual field evaluation indicated a complete bilateral left hemianopia with macular splitting. The patient had a constant alternating comitant exotropia with no suppression. By terminating the patching, establishing the appropriate fixing eye, and applying relieving prisms, diplopia was removed. Once binocularity was thus established, it was found (over the course of 7 months) that binocular function was possible with diminishing amounts of prism power. During this 7-month period, measurements of the patient's heterophoria, motor fusion, and sensory fusion revealed that he adapted from his occlusion-induced exotropia toward an habitual heterophoria. Such vergence adaptation has been defined as orthophorization. The occurrence of vergence adaptation after sensory fusion indicates that sensory fusion plays an important role in the etiology of prism adaptation.
Am J Optom Physiol Opt 1986 Sep
PMID:Orthophorization after occlusion-induced exotropia. 377 26

A 10-month-old boy who presented with strabismus and symptoms of intracranial hypertension was found to have a pineoblastoma and a unilateral ocular retinoblastoma. Despite enucleation of the eye, subtotal removal of the pineoblastoma, and craniospinal axis irradiation, the patient died 6 months later from disseminated intracranial neoplasm. As there was no clinical evidence of bilateral retinoblastoma, this case may represent a forme fruste of the trilateral retinoblastoma complex. The clinicopathological features of this unusual syndrome are reviewed.
Neurosurgery 1985 Sep
PMID:Concurrent pineoblastoma and unilateral retinoblastoma: a forme fruste of trilateral retinoblastoma? 404 65

The use of vertical fixation disparity data in the management of patients with vertical heterophoria will be more appropriate and effective when the clinical characteristics of vertical fixation disparity measurements are better understood. In this study the reliability and stability of the vertical fixation disparity curve and the relation of the vertical fixation disparity data to refractive status, stereoacuity, and vertical heterophoria were investigated. The results indicate that although the shape of the vertical fixation disparity curve is stable and can be statistically represented by a straight line, the slope changes with time, more so over weeks and months than during the day, and has no significant relation with the refractive status, with the level of stereoacuity, or with the presence or absence of vertical heterophoria.
Am J Optom Physiol Opt 1985 Sep
PMID:Clinical evaluation of vertical fixation disparity. Part II. Reliability, stability, and association with refractive status, stereoacuity, and vertical heterophoria. 405 Sep 59


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