2 research outputs found

    Septo-optic Dysplasia- Case Report

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    The clinical triad of septo-optic dysplasia (SOD) comprises the absence of the septum pellucidum, congenital optic nerve dysplasia, and multiple endocrine disorders. When any two of these factors are present, the condition is defined as an incomplete form of SOD. The authors report the case of an incomplete form of SOD in a 9-year-old boy with low vision and nystagmus present from birth. The bilateral ophthalmoscopic examination revealed small papillae with double contour images. Magnetic resonance imaging showed hypoplasia of the optic nerve bilaterally, chiasm and absence of the septum pellucidum.674653655De Morsier, G., Études sur les dysraphies cranio-encéphaliques. III. Agénésie du septum pellucidum avec malformation du tractus optique: La dysplasie septo-optique (1956) Schweiz Arch Neurol Psychiatr, 77 (1-2), pp. 267-292. , Texto inglês: [Studies on malformation of cranio-encephalic sutures.III. Agenesis of the septum lucidum with malformation of the optic tractKaplan, S., Grumbach, M.M., Hoyt, W., The syndrome of hypopituitary dwarfism, hypoplasia of optic nerves and malformation of prosencephalon: Report of 6 patients (1970) Pediatr Res, 4, pp. 480-481Lippe, B., Kaplan, S.A., La Franchi, S., Septo-optic dysplasia and maternal age (1979) Lancet, 2 (8133), pp. 92-93Purdy, F., Maternal factors in septo-optic dysplasia (1979) J Pediatr, 95 (4), p. 661Lambert, S.R., Hoyt, C.S., Narahara, M.H., Optic nerve hypoplasia (1987) Surv Ophthalmol, 32 (1), pp. 1-9Davis, G.V., Shock, J.P., Septo-optic dysplasia associated with see-saw nystagmus (1975) Arch Ophthalmol, 93 (2), pp. 137-139Williams, J., Brodsky, M.C., Griebel, M., Glasier, C.M., Caldwell, D., Thomas, P., Septo-optic dysplasia: The clinical insignificance of an absent septum pellucidum (1993) Dev Med Child Neurol, 35 (6), pp. 490-501Willnow, S., Kiess, W., Butenandt, O., Dörr, H.G., Enders, A., Strasser-Vogel, B., Endocrine disorders in septo-optic dysplasia (De Morsier syndrome) - evaluation and follow up of 18 patients (1996) Eur J Pediatr, 155 (3), pp. 179-18

    Disseminated Paracoccidioidomycosis With Chorioretinal Involvement [10]

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    [No abstract available]19910211023Silva, M.R., Mendes, R.P., Lastória, J.C., Barraviera, B., Marques, M.R., Kamegasawa, A., Paracoccidioidomycosis: Study of six cases with ocular involvement (1988) Mycopathologia, 102 (2), pp. 87-96Ajello, L., Polonelli, L., Imported paracoccidioidomycosis: A public health problem in non-endemic areas (1985) Eur J Epidemiol, 1 (3), pp. 160-165Bonomo, P.P., Belfort Jr., R., Tsunechiro, Jy., Filho, O.G., Choroidal granuloma caused by Paracoccidioides brasiliensis. A clinical and angiographic study (1982) Mycopathologia, 77 (1), pp. 37-41Negroni, R., Paracoccidioidomycosis (South American blastomycosis, Lutz's mycosis) (1993) Int J Dermatol, 32 (12), pp. 847-859Manns, B.J., Baylis, B.W., Urbanski, S.J., Gibb, A.P., Rabin, H.R., Paracoccidioidomycosis: Case report and review (1996) Clin Infect Dis, 23 (5), pp. 1026-1032Belfort Jr., R., Fishman, D.O., de Camargo, Z.P., Almada, A., Paracoccidioidomycosis with palpebral and conjunctival involvement (1975) Mycopathologia, 56 (1), pp. 21-24Arruda, W.O., Canto, M.A., Loddo, G., Rebuffi, V.F., Cardoso, M.A., Ocular paracoccidioidomycosis. Report of a case with posterior chorioretinitis (1986) Rev Inst Med Trop São Paulo, 28 (3), pp. 190-19
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