[Intra-lenticular metallic foreign bodies (apropos of 50 cases)].
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Biomedical subjects
Publications and source records attributed to P Turut.
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About 13 observations of sexe linked juvenile retinoschisis, the authors describe the ophthalmoscopic, fluorographic and functional aspects of the disease whose caracteristics are:--its sexe linked recessive heredity; --its clinical characterestics associating: a microcystic macular degeneration, peripheral retinal lesions, vitreous body alterations, --an electroretinogram of the negative type.
Macular alterations in pigmentary retinopathy may be divised into three groups: 1) Macular lesions in global tapeto retinal degeneration in Leber's disease with a chorioretinal aplasia involving at once both central peripheric retina. 2) Late macular degenerative phenomenons associated to pigmentary retinopathy, and presenting various ophthalmoscopic aspects. --atrophic macular degeneration;--isolated microkystic macular degeneration;--lamellar hote;--microkystic macular degeneration involving vitreous modifications (Goldmann-Favre's disease). 3) Kystoidal macular oedema in pigmentary retinopathy. These different aspects are studied on the ophthalmoscopic, fluorographic, functional, genetic and anatomo-pathologic points of view from our personnal study and a survey of the different observations found in literature. Their ethiopathogenesis remains hypothetic.
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