What can cause retinopathy?

Hypertension albinism candidiasis cat scratch disease tuberous sclerosis Patau syndrome Gaucher's disease retinoblastoma neurofibromatosis type I Chloroquine von Hippel-Lindau syndrome Familial adenomatous polyposis uveal melanoma Rift Valley fever Alström Syndrome Harlequin type ichthyosis Walker-Warburg syndrome Aceruloplasminemia glutathione synthetase deficiency AIDS Hunter syndrome Tamoxifen Alport syndrome Subacute sclerosing panencephalitis Laurence-Moon syndrome Vitamin E deficiency thioridazine incontinentia pigmenti Alagille syndrome deferoxamine Cockayne syndrome Aicardi syndrome Ceroid lipofuscinosis neuronal 2 late infantile macular hole Cohen Syndrome Norrie disease Mucolipidosis type IV Bietti's crystalline dystrophy Revesz syndrome Familial exudative vitreoretinopathy, autosomal dominant Jeune thoracic dystrophy syndrome Fleck retina of Kandori Congenital hyperplasia of retinal pigment epithelium Irvine-Gass syndrome Essential hypertension Foreign body, intraocular Pseudoxanthoma elasticum dominant type 1 Pseudoxanthoma elasticum dominant type 2 Ornithine ketoacid transaminase deficiency Miliary aneurysms of retina Lattice degeneration of retina Cone-rod retinal dystrophy Choroidal rupture Optic pit Goldmann-Favre syndrome.

Von Hippel-Lindau syndrome von Hippel-Lindau syndrome von Hippel-Lindau syndrome (an autosomal dominant disorder caused by mutations in a tumor suppressor gene) wikipedia Familial adenomatous polyposis Familial adenomatous polyposis Familial adenomatous polyposis, an inherited condition in which numerous polyps form mainly in the epithelium of the large intestine wikipedia uveal melanoma uveal melanoma uveal melanoma, cancer of the eye involving the iris, ciliary body, or choroid with advanced tumors encompassing more than one of these structures wikipedia Rift Valley fever Rift Valley fever Rift Valley Fever, a viral zoonosis causing fever wikipedia Alström Syndrome Alström Syndrome Alström syndrome, the rare genetic disorder caused by mutations in the gene ALMS1 wikipedia Harlequin type ichthyosis Harlequin type ichthyosis Harlequin-type ichthyosis, a skin disease, a most severe form of congenital ichthyosis, characterized by a thickening of the keratin layer in fetal human skin wikipedia Walker-Warburg syndrome Walker-Warburg syndrome Walker-Warburg syndrome, a rare form of autosomal recessive congenital muscular dystrophy associated with brain and eye abnormalities wikipedia Aceruloplasminemia Aceruloplasminemia Aceruloplasminemia, an autosomal recessive disorder characterized by progressive neurodegeneration of the retina and basal ganglia and diabetes mellitus wikipedia glutathione synthetase deficiency glutathione synthetase deficiency glutathione synthetase deficiency, a rare, autosomal recessive metabolic disorder that prevents the production of glutathione wikipedia AIDS AIDS AIDS the event wikipedia Hunter syndrome Hunter syndrome, or mucopolysaccharoidosis Type II, a lysosomal storage disease caused by a deficient enzyme, iduronate-2-sulfatase Tamoxifen Tamoxifen, the antagonist of the estrogen receptor in breast tissue via its active metabolite, 4-hydroxytamoxifen wikipedia Alport syndrome Alport syndrome, a genetic disorder characterized by glomerulonephritis, endstage kidney disease, and hearing loss wikipedia Subacute sclerosing panencephalitis Subacute sclerosing panencephalitis, a rare chronic, progressive encephalitis that affects primarily children and young adults, caused by a persistent infection of immune resistant measles virus wikipedia Laurence-Moon syndrome Laurence-Moon syndrome (a syndrome of mental retardation, retinitis pigmentosa, hypogonadism, and spastic paraplegia) Vitamin E deficiency Vitamin E deficiency causes nerve problems due to poor conduction of electrical impulses along nerves due to changes in nerve membrane structure and function wikipedia thioridazine Thioridazineis a piperidine typical antipsychotic drug belonging to the phenothiazine drug group and previously widely used in the treatment of schizophrenia and psychosis wikipedia incontinentia pigmenti incontinentia Pigmenti, a genetic disorder that affects the skin, hair, teeth, and nails wikipedia Alagille syndrome Alagille syndrome, a genetic disorder that affects the liver, heart, and other systems of the body wikipedia deferoxamine Deferoxamine, a chelating agent used to remove excess iron from the body wikipedia Cockayne syndrome Cockayne syndrome, a rare, autosomal recessive disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight, and premature aging wikipedia Aicardi syndrome Aicardi syndrome, an uncommon malformation syndrome characterized by absence of a key structure in the brain called the corpus callosum, a presence of retinal abnormalities, and seizures in the form of infantile spasms wikipedia Ceroid lipofuscinosis neuronal 2 late infantile Ceroid lipofuscinosis neuronal 2 late infantile (this type is caused by mutation in the cln2 gene encoding tripeptidyl-peptidase I, a lysosomal serine protease) macular hole macular hole, a small break in the macula, located in the center of the eye's light-sensitive tissue called the retina wikipedia Cohen Syndrome Cohen syndrome, believed to be a gene mutation at locus 8q22 gene COH1 wikipedia Norrie disease Norrie Disease, a genetic disorder that primarily affects the eye and almost always leads to blindness wikipedia Mucolipidosis type IV Mucolipidosis type IV, like other types of mucolipidosis, an inherited neurodegenerative lysosomal storage disorder wikipedia Bietti's crystalline dystrophy Bietti's crystalline dystrophy, also called Bietti's crystalline retinopathy, a rare autosomal recessive eye disease named for Dr. G. B. Bietti wikipedia Revesz syndrome Revesz syndrome, a fatal disease that causes exudative retinopathy and bone marrow failure wikipedia Familial exudative vitreoretinopathy, autosomal dominant Familial exudative vitreoretinopathy, autosomal dominant, the cause and medical concept with DiseasesDB code "32973" Jeune thoracic dystrophy syndrome Jeune thoracic dystrophy syndrome (congenital polychondrodystrophy in which narrow and rigid thoracic cage results in asphyxia, ranging in severity from mild cases with minimal respiratory symptoms to fatal asphyxiation) Fleck retina of Kandori Fleck retina of Kandori, the cause and medical concept with DiseasesDB code "32762" Congenital hyperplasia of retinal pigment epithelium Congenital hyperplasia of retinal pigment epithelium, the cause and medical condition with DiseasesDB code "32925" Irvine-Gass syndrome Irvine-Gass syndrome, the cause and medical concept with Mesh code "D008269" and DiseasesDB code "32406" Essential hypertension Essential hypertension (hypertension occurring without preexisting renal disease or known organic cause) Foreign body, intraocular Foreign body, intraocular, the cause and medical concept with DiseasesDB code "4927" Pseudoxanthoma elasticum dominant type 1 Pseudoxanthoma elasticum dominant type 1, the cause and medical concept with DiseasesDB code "10876" Pseudoxanthoma elasticum dominant type 2 Pseudoxanthoma elasticum dominant type 2, the cause and medical concept with DiseasesDB code "10881" Ornithine ketoacid transaminase deficiency Ornithine ketoacid transaminase deficiency (progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood) Miliary aneurysms of retina Miliary aneurysms of retina, the cause and medical concept with DiseasesDB code "31162" Lattice degeneration of retina Lattice degeneration of retina, the cause and medical concept with DiseasesDB code "31274" Cone-rod retinal dystrophy Cone-rod retinal dystrophy, the cause and medical concept with DiseasesDB code "31284" Choroidal rupture Choroidal rupture, the cause and medical concept with DiseasesDB code "31303" Optic pit Optic pit, the cause and medical concept with DiseasesDB code "31315" Goldmann-Favre syndrome Goldmann-Favre syndrome, the cause and medical concept with DiseasesDB code "31755.

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