Academic Journal

Evanescent white linear flecks and posterior microphthalmos: new features of a recently established disease

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Evanescent white linear flecks and posterior microphthalmos: new features of a recently established disease
Συγγραφείς: Tran, H. V., Borruat, F. X., Reymond-Gruber, S., Schorderet, D., Munier, F.
Έτος έκδοσης: 2006
Συλλογή: Université de Lausanne (UNIL): Serval - Serveur académique lausannois
Θεματικοί όροι: Child Child, Preschool Humans Infant Male Microphthalmos/*classification/complications/*diagnosis Retinal Diseases/classification/*congenital/*diagnosis Vision Disorders/classification/*congenital/*diagnosis
Περιγραφή: BACKGROUND: Posterior microphthalmos is a rare autosomal recessive condition with normal anterior segment and small posterior segment resulting in axial hyperopia and retinal folding. HISTORY AND SIGNS: The proband from a consanguineous Turkish family was clinically investigated at 5 months of age and followed for the next 8 years. At five months of age, refraction revealed a severe hyperopia of + 10 diopters in both eyes (OU) with a mean axial length of 16.5 mm. Fundus examination showed a dystrophic maculo-papillar bundle. Multiple whitish deep intraretinal linear lesions sparing the macula were present in the mid-periphery with no preferential orientation. THERAPY AND OUTCOME: By 8 years of age, visual acuity was 20/25 in the right eye (OD) and 20/30 in the left eye (OS) with S + 14 OU. The whitish linear lesions had disappeared and were replaced by retinal pigment epithelium alterations. Optical coherence tomography (OCT) revealed a thickened retina with normal appearance at the site of the linear lesions. CONCLUSIONS: This is the first report of long-term follow-up and OCT findings in this rare ocular developmental abnormality.
Τύπος εγγράφου: article in journal/newspaper
Γλώσσα: unknown
ISSN: 0023-2165
Relation: Klinische Monatsblätter für Augenheilkunde; https://iris.unil.ch/handle/iris/109219; serval:BIB_299763CD25BB; 000238027900015
DOI: 10.1055/s-2006-926563
Διαθεσιμότητα: https://iris.unil.ch/handle/iris/109219
https://doi.org/10.1055/s-2006-926563
Αριθμός Καταχώρησης: edsbas.1D6DF451
Βάση Δεδομένων: BASE
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  Data: Evanescent white linear flecks and posterior microphthalmos: new features of a recently established disease
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  Data: <searchLink fieldCode="AR" term="%22Tran%2C+H%2E+V%2E%22">Tran, H. V.</searchLink><br /><searchLink fieldCode="AR" term="%22Borruat%2C+F%2E+X%2E%22">Borruat, F. X.</searchLink><br /><searchLink fieldCode="AR" term="%22Reymond-Gruber%2C+S%2E%22">Reymond-Gruber, S.</searchLink><br /><searchLink fieldCode="AR" term="%22Schorderet%2C+D%2E%22">Schorderet, D.</searchLink><br /><searchLink fieldCode="AR" term="%22Munier%2C+F%2E%22">Munier, F.</searchLink>
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  Data: Université de Lausanne (UNIL): Serval - Serveur académique lausannois
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  Data: <searchLink fieldCode="DE" term="%22Child+Child%22">Child Child</searchLink><br /><searchLink fieldCode="DE" term="%22Preschool+Humans+Infant+Male+Microphthalmos%2F*classification%2Fcomplications%2F*diagnosis+Retinal+Diseases%2Fclassification%2F*congenital%2F*diagnosis+Vision+Disorders%2Fclassification%2F*congenital%2F*diagnosis%22">Preschool Humans Infant Male Microphthalmos/*classification/complications/*diagnosis Retinal Diseases/classification/*congenital/*diagnosis Vision Disorders/classification/*congenital/*diagnosis</searchLink>
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  Data: BACKGROUND: Posterior microphthalmos is a rare autosomal recessive condition with normal anterior segment and small posterior segment resulting in axial hyperopia and retinal folding. HISTORY AND SIGNS: The proband from a consanguineous Turkish family was clinically investigated at 5 months of age and followed for the next 8 years. At five months of age, refraction revealed a severe hyperopia of + 10 diopters in both eyes (OU) with a mean axial length of 16.5 mm. Fundus examination showed a dystrophic maculo-papillar bundle. Multiple whitish deep intraretinal linear lesions sparing the macula were present in the mid-periphery with no preferential orientation. THERAPY AND OUTCOME: By 8 years of age, visual acuity was 20/25 in the right eye (OD) and 20/30 in the left eye (OS) with S + 14 OU. The whitish linear lesions had disappeared and were replaced by retinal pigment epithelium alterations. Optical coherence tomography (OCT) revealed a thickened retina with normal appearance at the site of the linear lesions. CONCLUSIONS: This is the first report of long-term follow-up and OCT findings in this rare ocular developmental abnormality.
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  Data: Klinische Monatsblätter für Augenheilkunde; https://iris.unil.ch/handle/iris/109219; serval:BIB_299763CD25BB; 000238027900015
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