Differential (Click to cross reference) acanthocytosis adrenoleukodystrophy adverse drug reaction ataxia, cerebellar Bassen-Kornzweig syndrome behavioral disorder blindness cataracts cerebro hepato renal syndrome Cockayne's syndrome consanguinity cornea, abnormal deafmute deafness DNA probes drug induced neurologic disorders dwarfism electroencephalogram, abnormalities of electronystagmography electroretinograph Friedreich's ataxia fundus, abnormality of gargoylism genetic linkage genetic neurologic disorders glaucoma Hallervorden Spatz disease Hallgren's syndrome heart block Hurler's syndrome Kearns-Sayre syndrome keratoconus Laurence-Moon-Bardet-Biedl syndrome macular degeneration malformation, CNS, congenital mental retardation mucopolysaccharidoses myopathy, mitochondrial myopia neuritis neurologic disease, diagnoses of neuronal ceroid-lipofuscinosis neuropathy neuropathy, hereditary peripheral night blindness nystagmus nystagmus, pendular obesity ocular myopathy optic atrophy optic nerve optic neuropathy peroxisomal disease pigmentary retinopathy polydactyly prognosis pseudoretinitis pigmentosa psychiatric disorder pupil, abnormality in neurologic disorders pupil, light reflex, abnormal refractive errors Refsum's disease retinal degeneration retinal lesion retinitis pigmentosa retinopathy review article roving eye movements schizophrenia seizure sensorineural hearing loss Spielmeyer Vogt syndrome spinocerebellar degeneration tapetoretinal degeneration treatment of neurologic disorder Usher's syndrome visual acuity, decreased visual field defect visual fields, constricted visual loss

Showing articles 0 to 3 of 3 Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Tapetoretinal Degeneration in Childhood Presenting as a Disturbance of Behavior BMJ 202, 1972 Jan., Harcourt,B.,et al, 1972 Genetic Counseling in Retinitis Pigmentosa MCV Quart 8:283, Noah,V., 1972 Showing articles 0 to 3 of 3