{"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\/es\/pediatric-retinal-diseases\/","title":{"rendered":"Enfermedades pedi\u00e1tricas de la retina"},"content":{"rendered":"
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Enfermedades pedi\u00e1tricas de la 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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Enfermedad 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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Vitreorretinopat\u00eda exudativa 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> Vitreorretinopat\u00eda exudativa familiar (FEVR)<\/span><\/a>\n\t\t<\/div>

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Enfermedad 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
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S\u00edndrome de 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 de vasculatura fetal persistente (SVFP)<\/span><\/a>\n\t\t<\/div>

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Retinopat\u00eda del prematuro (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> Retinopat\u00eda del prematuro (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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