{"id":6486,"date":"2024-10-22T19:21:29","date_gmt":"2024-10-22T19:21:29","guid":{"rendered":"https:\/\/prrf.org\/?page_id=6486"},"modified":"2025-10-24T22:20:53","modified_gmt":"2025-10-24T22:20:53","slug":"pediatric-retinal-diseases","status":"publish","type":"page","link":"https:\/\/prrf.org\/pt\/pediatric-retinal-diseases\/","title":{"rendered":"Doen\u00e7as pedi\u00e1tricas da retina"},"content":{"rendered":"
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Doen\u00e7as pedi\u00e1tricas da retina<\/h1><\/div>\n\t\t<\/div> \n\t<\/div>\n\t<\/div> \n<\/div><\/div>\n\t\t\t<\/div> \n\t\t<\/div>\n\t<\/div> \n<\/div><\/div>\n\t\t
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Doen\u00e7a de Coats<\/h3>\n
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Coats’ disease is a rare eye condition where the tiny blood vessels in the retina develop abnormally. The retina is the light-sensitive layer at the back of your eye that acts like the film in a camera, sending visual messages to your brain.<\/p>\n<\/div>\n<\/div> Coats' Disease<\/span><\/a>\n\t\t<\/div>

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Vitreoretinopatia Exsudativa Familiar (FEVR)<\/h3>\n
Familial Exudative Vitreoretinopathy, or FEVR, is a rare genetic eye condition that affects the development of blood vessels in the retina, whereby the blood vessels at the edges…<\/div>\n<\/div> Vitreoretinopatia Exsudativa Familiar (FEVR)<\/span><\/a>\n\t\t<\/div>

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Doen\u00e7a de Norrie<\/h3>\n
Norrie Disease is a rare genetic disorder that primarily affects males, leading to blindness at birth and often hearing loss and developmental challenges as children grow. The condition was first described in 1961 by Danish ophthalmologist Mette Warburg…<\/div>\n
<\/div>\n<\/div> Doen\u00e7a de Norrie<\/span><\/a>\n\t\t<\/div>

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S\u00edndrome da Vasculatura Fetal Persistente (SVFP)<\/h3>\n
Persistent Fetal Vasculature Syndrome (PFVS) is a rare eye condition present at birth. It occurs when certain blood vessels in the eye, which are supposed to disappear…<\/div>\n
<\/div>\n<\/div> S\u00edndrome da Vasculatura Fetal Persistente (SVFP)<\/span><\/a>\n\t\t<\/div>

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Retinopatia da prematuridade (ROP)<\/h3>\n
Retinopathy of prematurity (ROP), often called “ROP,” is an eye disease that can affect babies born too early (prematurely). It happens because the blood vessels in the retina haven’t finished growing when the baby is born.<\/div>\n<\/div> Retinopatia da prematuridade (ROP)<\/span><\/a>\n\t\t<\/div>

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Congenital X\u2011Linked Retinoschisis<\/h3>\n
Congenital X-Linked Retinoschisis, often referred to as XLRS, is a genetic eye condition that primarily affects males. It causes a splitting (the “schisis” part of the name) of the layers of the retina.<\/div>\n<\/div> Congenital X\u2011Linked Retinoschisis<\/span><\/a>\n\t\t<\/div>

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S\u00edndromes de Stickler<\/h3>\n
Stickler syndrome is a genetic condition which primarily affects the collagen in the body – a key building block for many of our tissues, like cartilage, joints, eyes, and ears. Because collagen is so widespread, Stickler syndrome can affect…<\/div>\n<\/div> S\u00edndromes de Stickler<\/span><\/a>\n\t\t<\/div>

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S\u00e9rie de v\u00eddeos educativos do PRRF<\/h2>\n\t<\/div>\n<\/div>\n\n\n\n\n\t\t<\/div> \n\t<\/div>\n\t<\/div> \n<\/div><\/div>
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