本文へスキップ

小児網膜疾患

Young visually impaired boy in a colorful ball pit

コート病

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

さらに詳しく

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

家族性滲出性硝子体網膜症（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…
家族性滲出性硝子体網膜症（FEVR）

さらに詳しく

A young boy with red glasses listening to a wooden xylophone

ノリー病

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…
ノリー病

さらに詳しく

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

持続性胎児血管症候群（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…
持続性胎児血管症候群（PFVS）

さらに詳しく

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

未熟児網膜症（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.
未熟児網膜症（ROP）

さらに詳しく

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

さらに詳しく

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

スティクラー症候群

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…
スティクラー症候群

さらに詳しく

PRRF教育ビデオシリーズ

未熟児網膜症の驚くべき進歩

マイケル・トレセ博士が未熟児網膜症（ROP）の驚くべき進歩について語る。

PRRFの使命を追求することの重要性

マイケル・トレース医師は、PRRFの使命を追求することが、子どもたち、家族、そして未来の患者たちの未来にとって非常に重要である理由を語っている。

網膜疾患の原因

小児網膜研究所所長のケン・ミトン博士が、網膜疾患の原因を特定する方法について語る。

DNA変異体を見つける

小児網膜研究所技師のウェンディ・ダイリーは、患者のDNA変異を見つける方法を説明している。

希少疾病とは何か？

キンバリー・ドレンザー博士が、希少疾病と呼ばれる理由と、製薬会社やFDAがこの疾病をどのように見ているかを語る。

Help us find a cure!

ja日本語
en_USEnglish es_MXEspañol de México fr_FRFrançais de_DEDeutsch nl_NLNederlands pt_PTPortuguês zh_CN简体中文 ru_RUРусский it_ITItaliano ja日本語