Preretinal and Intraretinal Exudates in Familial Exudative Vitreoretinopathy

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Familial Exudative Vitreoretinopathy

Familial exudative vitreoretinopathy (FEVR) is a hereditary disease associated with visual loss, particularly in the pediatric group. Mutations in the NDP, FZD4, LRP5, and TSPAN12 genes have been shown to contribute to FEVR. FEVR has been reported to have X-linked recessive, autosomal dominant, and autosomal recessive inheritances. However, both the genotypic and phenotypic features are variabl...

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Familial exudative vitreoretinopathy associated with familial thrombocytopathy.

Two families with familial exudative vitreoretinopathy were studied in which platelet aggregation defects were found in all the affected members. The major defect observed was absent platelet aggregation with arachidonic acid. In addition platelet aggregation with collagen and adrenaline was reduced in one severely affected member. The implication of the platelet aggregation defect in the patho...

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familial exudative vitreoretinopathy

purpose: to report a relatively rare case of familial exudative vitreoretinopathy (fevr). patient and findings: a 13-year-old boy referred with decreased visual acuity of both eyes, specially right eye from 6 years ago. he had several ophthalmologist and optometrist visits and spectacle prescription without any improvement of vision. best corrected visual acuity (bcva) was 25 cm of count finger...

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Excessive myopia and anisometropia associated with familial exudative vitreoretinopathy.

BACKGROUND To describe associations between familial exudative vitreoretinopathy (FEVR) and refractive status. METHODS We conducted retrospective studies of patients with clinical diagnoses of familial exudative vitreoretinopathy from June 1986 through September 2000. All patients had cycloplegic refraction, visual acuity with correction, and underwent fundus examination. Ocular history since...

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Familial Exudative Vitreoretinopathy: Presentation in the First Week of Life.

To the Editors: A male infant born at 36 weeks of gestation with a birth weight of 2,500 grams presented to our department at 37 weeks’ post-conceptional age. The infant was not admitted in any neonatal intensive care unit, had not received oxygen, and did not have a history of neonatal sepsis. He was otherwise healthy. The infant was brought for a retinal check-up because his elder sibling was...

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ژورنال

عنوان ژورنال: Retina

سال: 2011

ISSN: 0275-004X

DOI: 10.1097/iae.0b013e3182019c04