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小儿视网膜疾病

Young visually impaired boy in a colorful ball pit

高兹病

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.

Coats' Disease

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Young girl with glasses sitting on a swing and sticking her tongue out

家族性渗出性玻璃体视网膜病变（FEVR）

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…
家族性渗出性玻璃体视网膜病变（FEVR）

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A young boy with red glasses listening to a wooden xylophone

诺里病

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…
诺里病

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Young boy with glasses and a blue eye patch on one side smiles and gives a thumbs up

胎儿血管持续综合征（PFVS）

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…
胎儿血管持续综合征（PFVS）

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Visually impaired teenage girl sitting on the floor and hugging a black and white dog

早产儿视网膜病变（ROP）

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.
早产儿视网膜病变（ROP）

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Teenage boy sitting at a table and looking at the camera

Congenital X‑Linked Retinoschisis

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.
Congenital X‑Linked Retinoschisis

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Smiling young girl with brown curly hair holding a stuffed bunny toy

斯蒂克勒综合征

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…
斯蒂克勒综合征

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PRRF 教育视频系列

早产儿视网膜病变的惊人进展

迈克尔-特雷斯（Michael Trese）博士分享了早产儿视网膜病变（ROP）的惊人进展。

履行 PRRF 使命的重要性

迈克尔-特雷斯博士（Dr. Michael Trese）分享了追求 PRRF 的使命为何对儿童、家庭和未来患者的未来如此重要。

视网膜疾病的原因

小儿视网膜研究实验室主任 Ken Mitton 博士讨论如何确定视网膜疾病的病因。

寻找 DNA 变异体

小儿视网膜研究实验室技术员温迪-戴利（Wendy Dailey）解释了如何在患者体内发现 DNA 变异。

什么是孤儿病？

Kimberly Drenser 博士分享了为什么这些疾病被称为 "孤儿病"，以及制药公司和美国食品及药物管理局是如何看待这些疾病的。

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