Rx Eye & Vision Care (A – Z)
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Coloboma of the Choroid and Retina
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Coloboma of the choroid and retina (often called chorioretinal coloboma) is a birth defect of the back part of the eye. In this condition, there is a missing ...

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Nodular Unilateral Glaucoma
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Nodular unilateral glaucoma is a description, not an official single disease name. It usually means glaucoma in one eye (unilateral) that is caused or worsened ...

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Cogan-Reese Syndrome
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Cogan-Reese syndrome is a very rare eye disease. It affects the clear front window of the eye (the cornea), the colored part (the iris), and the fluid-drainage ...

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Cerebroretinal Microangiopathy with Calcifications and Cysts
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Cerebroretinal microangiopathy with calcifications and cysts is a very rare inherited disease that mainly damages the tiny blood vessels in the brain and the ...

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Choroiditis
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Choroiditis means inflammation in the choroid, which is a thin, rich blood-vessel layer under the retina at the back of the eye. This layer feeds the retina ...

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Tapetochoroidal Dystrophy
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Tapetochoroidal dystrophy is another name that has been used for choroideremia, an inherited eye disease that slowly damages the light-sensing retina and the ...

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Choroideremia
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Choroideremia is a rare eye disease that slowly takes away sight over many years. It mainly affects boys and men because the problem gene is on the X ...

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Regional Choroidal Atrophy and Alopecia
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Regional choroidal atrophy and alopecia (also called Moloney syndrome or choroidal atrophy–alopecia syndrome) is a very rare inherited condition. In this ...

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Choroidal Atrophy–Alopecia Syndrome
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Choroidal atrophy–alopecia syndrome is an extremely rare genetic condition in which a person has both damage and thinning of the choroid in the eye and loss of ...

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Chorioretinitis
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Chorioretinitis is swelling and irritation (inflammation) of two important layers at the back of the eye: the choroid (a layer rich in blood vessels) and the ...

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Channelopathy-Associated Congenital Insensitivity to Pain (CIP)
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Channelopathy-associated congenital insensitivity to pain is a very rare genetic condition where a person is born unable to feel physical pain, even when the ...

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Posterior Membrane Corneal Dystrophy
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Posterior membrane corneal dystrophy is a rare eye disease that mainly affects the deepest layer of the clear front window of the eye (the cornea) and the thin ...

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Endothelial Corneal Dystrophy
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Endothelial corneal dystrophy is a long-lasting eye disease that mainly damages the inner cell layer of the cornea, called the corneal endothelium. These cells ...

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Dystrophy of the Corneal Endothelium
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Dystrophy of the corneal endothelium is a long-lasting (chronic) disease of the inner layer of the clear front window of the eye, called the cornea. In this ...

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Chandler Syndrome
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Chandler syndrome is a rare eye disease that affects the clear front window of the eye (the cornea), the colored part (the iris), and the drainage angle where ...

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Central Serous Retinopathy (CSR)
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Central serous retinopathy (CSR) is an eye disease where fluid collects under the central part of the retina and makes central vision blurry or distorted. It ...

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Central Serous Choroidopathy
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Central serous choroidopathy, more commonly called central serous chorioretinopathy (CSC), is an eye disease that affects the macula, the central part of the ...

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Central Serous Chorioretinopathy
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Central serous chorioretinopathy is an eye disease where fluid leaks from tiny blood vessels under the retina (the light-sensitive “camera film” at the back of ...

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Central Cloudy Dystrophy of François
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Central cloudy dystrophy of François (often shortened to CCDF) is a very rare corneal condition where the clear window of the eye (the cornea) develops faint, ...

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Central Cloudy Corneal Dystrophy of François (CCDF)
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Central cloudy corneal dystrophy of François (CCDF) is a very rare problem of the cornea (the clear “window” at the front of the eye). In CCDF, doctors see ...

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