In June 1946 Moreau developed choroiditis which threatened his eyesight.

This type of uveitis is called choroiditis.

Afterwards this disorder was referred to as "Doyne's honeycomb choroiditis".

Types of uveitis are iritis, cyclitis, retinitis, and choroiditis.

If only the choroid is inflamed and not the retina, the condition is termed choroiditis.

Posterior uveitis, also known as choroiditis, refers to inflammation of the choroid, the back part of the uvea.

Multifocal choroiditis with panuveitis: incidence of ocular complications and loss of visual acuity.

Ocular manifestations, such as photophobia, hyperlacrimation, iritis, iridocyclitis, choroiditis and blindness have also been described.

(Lessons on inflammatory diseases of the internal membranes of the eye including iritis, choroiditis, and glaucoma.

Multifocal choroiditis (MCP)

See uveitis, choroiditis, iritis, Iridocyclitis, anterior uveitis, sympathetic ophthalmia, uveal melanoma.

In December, 1922 he first reported "A case of acute diffuse choroiditis with retinal detachment" at a meeting of ophthalmologists in Tokyo.

Other conditions that can present with complaints of metamorphopsia include pathological myopia, presumed ocular histoplasmosis syndrome, choroidal rupture and multifocal choroiditis.

The condition sometimes described erroneously as myopic choroiditis, but myopic crescent is not an inflammatory process and does not run parallel to the degree of myopia.

Punctate inner choroiditis (PIC) is an inflammatory choroiditis which occurs mainly in young women.

In contrast, white dots appear later in the disease stages of birdshot choroidopathy, serpiginous choroiditis, and APMPPE.

Serpiginous choroiditis, also known as geographic or helicoid choroidopathy, is an uncommon chronic progressive inflammatory disease affecting adult men and women equally in the second to seventh decades of life.

Serpiginous Choroiditis is a rare recurrent eye disorder characterized by irregularly shaped (serpiginous) lesions involving two layers of the eye surface (the retinal pigment epithelium and the choriocapillaris).

There are numerous conditions leading to uveitis, and many have floaters and blurred vision as predominant symptoms: sarcoidosis, toxoplasmosis chorioretinitis, ocular histoplasmosis, multifocal choroiditis, pars planitis, endophalmitis, syphilis, candidiasis, viral uveitis, Vogt-Koyanagi-Harada syndrome, and HIV related unveitis.

Multifocal choroiditis and panuveitis (MCP) is an idiopathic inflammatory disorder of unknown etiology affecting the choroid, retina, and vitreous of the eye that presents asymmetrically, most often in young myopic women with photopsias, enlargement of the physiologic blind spot and decreased vision.