Pediatric Ophthalmology, Volume 2 |
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Results 1-3 of 81
Page 769
... peripheral nasal quadrants lying medial to those from the peripheral temporal quadrants . In the more proximal portion of the optic nerve ( proximal to the level of en- trance of the central retinal vessels ) the papillomacular bundle ...
... peripheral nasal quadrants lying medial to those from the peripheral temporal quadrants . In the more proximal portion of the optic nerve ( proximal to the level of en- trance of the central retinal vessels ) the papillomacular bundle ...
Page 775
... peripheral isopters is reduced to absolute blindness , leaving the whole field equally restricted , generalized peripheral contrac- tion or concentric contraction exists . Generalized field depression can be demonstrated in normal ...
... peripheral isopters is reduced to absolute blindness , leaving the whole field equally restricted , generalized peripheral contrac- tion or concentric contraction exists . Generalized field depression can be demonstrated in normal ...
Page 793
... peripheral nerves . 12. Refsum's Syndrome - Peripheral polyneuropathy , cerebellar ataxia , retinitis pigmentosa , spinal fluid protein ele- vation . - In some cases , ichthyosis . - In certain instances , PEO . - Autosomal recessive ...
... peripheral nerves . 12. Refsum's Syndrome - Peripheral polyneuropathy , cerebellar ataxia , retinitis pigmentosa , spinal fluid protein ele- vation . - In some cases , ichthyosis . - In certain instances , PEO . - Autosomal recessive ...
Contents
PEDIATRIC NEUROOPHTHALMOLOGY | 767 |
Pupil Abnormalities | 783 |
DISORDERS OF THE LIDS 412 | 793 |
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Common terms and phrases
abnormalities acid affected Albinism Amer antibodies antigens Arch associated autoimmune autosomal bilateral blindness C. V. Mosby cataracts cause cells cent cerebral child childhood choroid clinical congenital conjunctiva corneal cranial cyst cystinosis defect deficiency degeneration develop diabetes diagnosis disc disorder drome Duke-Elder dystrophy edema enzyme errors of metabolism Fabry's disease familial fibers fixation frequently fundus Gaucher's disease gaze genetic glaucoma glioma hemorrhage hereditary homocystinuria hypoplasia immune Inborn Errors infection intracranial intraocular involvement iris keratitis lens lenses lesions lipid lymphocytes macrophages macular malignant membrane ment muscle neurologic Niemann-Pick disease normal nystagmus occur ocular manifestations Ophthal Ophthalmology optic atrophy optic nerve optic neuritis orbital palsy papilledema pathologic patients pediatric peripheral pigment pigmentary posterior primary protein ptosis pupillary renal response result retinal detachment retinoblastoma serum signs skin strabismus symptoms syndrome Systemic Table therapy tion tissue trauma treatment tumor usually uveitis vascular vision visual acuity vitamin vitreous