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Titlebook: Handbook of Pediatric Retinal Disease; Kenneth W. Wright (Director and Clinical Professor Book 2006 Springer-Verlag New York 2006 care.dia

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Breaking the News: The Role of the Physician,and Brian, age 3 months, their long-awaited son. At Brian’s 3-month routine well-baby checkup, the pediatrician remarked that Brian might have strabismus because his eyes appeared to turn in and weren’t “working together,” as Janet later described it. The pediatrician was very reassuring, however, a
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,Heritable Disorders of RPE, Bruch’s Membrane, and the Choriocapillaris,t of many of these conditions is the accumulation of yellowish material within and beneath the retinal pigment epithelium (RPE) associated with a progressive loss of macular RPE cells. A number of toxic and inflammatory conditions can also cause dots and spots at the level of the RPE, but these cond
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Disorders of the Vitreous and Vitreoretinal Interface,fold of cross-linked collagen fibrils with hyaluronic acid molecules within the scaffold. Hyaluronic acid is very hydrophilic, and water molecules are attracted to the scaffold providing turgor and rigidity to the matrix. The vitreous is primarily a solid gel in children’s eyes but becomes progressi
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Retinoblastoma and Other Malignant Intraocular Tumors,ing, early diagnosis, and treat- ment. In fact, we are convinced that in the coming decades detecting early disease by lowering the average age at initial diagnosis will prove to be a much more efficient and cost- effective way to manage retinoblastoma than developing exotic new drugs or gene therap
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Retinopathy of Prematurity,the development of vascular shunts, neovascularization, and, in its more severe forms, traction retinal detachment. The development of retinal vascular shunts and neovascularization in ROP is believed to be related to local ischemia, which is a predominant feature of other proliferative retinopathie
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