نتایج جستجو برای: ocular abnormalities

تعداد نتایج: 156050  

Journal: :Annals of optometry and contact lens 2022

A scleral contact lens lies on the sclera, not cornea, which differs from a rigid gas permeable (RGP) lens, and has shown successful clinical outcomes in patients unable to tolerate glasses or RGP lenses because of severely deformed cornea. In addition, forms tear film between cornea that stabilizes ocular surface could be useful therapeutic option. The mini-scleral is option for visual improve...

Journal: :American journal of ophthalmology 1976
S Brownstein T H Kirkham D K Kalousek

A 920-g male infant born with features of Potter's syndrome had multiple ocular anomalies. Ocular abnormalities included absence of keratocytes in the inner central corneal stroma, cataract with retention of cell nuclei in the nucleus of the lens, hypoplasia of the ganglion cell and nerve fiber layers of the retina, and absence of nerve bundles in the optic nerve. Other ocular findings includin...

Journal: :International Journal of Contemporary Pediatrics 2021

Background: Cerebral palsy (CP) describes a group of permanent disorder the development movement and posture, causing activity limitation, that are attributed to non-progressive disturbance occurred in developing fetal or infant brain. The motor disorders cerebral often accompanied by disturbances sensation, perception, cognition, communication behavior, epilepsy, secondary musculoskeletal prob...

Journal: :Neurologic clinics 2010
Sashank Prasad Nicholas J Volpe

Eye movement abnormalities constitute an important clinical sign that can be a manifestation of dysfunction of cranial nerves III, IV, and VI (the 3 ocular motor nerves). Specific motility deficits often have highly localizing value within the neuroaxis, serving to refine a differential diagnosis and guide management. This article reviews the key anatomic concepts, clinical presentation, differ...

Journal: :Indian Journal of Obstetrics and Gynecology Research 2022

Joubert syndrome is a rare autosomal recessive inherited disease associated with many signs and symptoms. (JS) was first discovered by Marie in 1969. Joubert’s presents as low muscle tone (hypotonia), have difficulty coordinating movements (ataxia), episodes of fast or slow breathing abnormal eye movement (ocular motor apraxia). Developmental delay intellectual disability generally accompany. A...

Journal: :The British journal of ophthalmology 1982
J R Cruysberg A F Deutman

Three patients had during pregnancy visual disturbances caused by central serous choroidopathy. One of them had a central scotoma in her first and second pregnancy. The 2 other patients had a central scotoma in their first pregnancy. Symptoms disappeared spontaneously after delivery. Except for the ocular abnormalities the pregnancies were without complications. The complaints can be misinterpr...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید

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