University of Iowa Health Care

Ophthalmology and Visual Sciences

EyeRounds.org

EyeRounds Online Atlas of Ophthalmology

Inherited Eye Diseases

(Category added to the EyeRounds Atlas, 2013)

Click on the thumbnail images for a larger photograph and description of each case

Photograph Diagnosis
Aicardi Syndrome Aicardi syndrome
Autosomal dominant neovascular inflammatory vitreoretinopathy (ADNIV) Autosomal dominant neovascular inflammatory vitreoretinopathy (ADNIV)
Autosomal Recessive Best Disease Autosomal recessive Best disease
Axenfeld-Rieger Syndrome Axenfeld-Rieger Syndrome
Axenfeld-Rieger syndrome Axenfeld-Rieger Syndrome
Bardet-Biedl Bardet-Biedl Syndrome
Batten Disease Batten Disease
Choroideremia Choroideremia
Congenital aniridia Congential aniridia
Congenital aniridia Congential aniridia


Congenital Aniridia, Boston Keratoprosthesis (KPro)

Congenital Aniridia and Boston Keratoprosthesis (KPro)
Dominant optic atrophy Dominant optic atrophy
Enhanced S-cone Syndrome Enhanced S-Cone Syndrome
Erosive vitreoretinopathy Erosive vitreoretinopathy
Familial Exudative Vitreoretinopathy (FEVR) Familial Exudative Vitreoretinopathy (FEVR)
Familial Exudative Vitreoretinopathy (FEVR) Familial Exudative Vitreoretinopathy (FEVR)
Familial Exudative Vitreoretinopathy (FEVR) Familial Exudative Vitreoretinopathy (FEVR)
Granular corneal dystrophy, type 1 Granular corneal dystrophy type 1
Granular corneal dystrophy Granular corneal dystrophy
Gyrate Atrophy Gyrate atrophy
Involuted choroidal neovascular membrane (CNVM) mimicking a granuloma in pseudoxanthoma elasticum (PXE) Involuted choroidal neovascular membrane (CNVM) mimicking a granuloma in pseudoxanthoma elasticum (PXE)
Lattice Corneal Dystrophy Lattice corneal dystrophy
LCHADD: long chain 3-hydroxyacyl CoA dehydrogenase deficiency LCHADD: long chain 3-hydroxyacyl CoA dehydrogenase deficiency
Leber Congenital Amaurosis, RPE65-associated Leber Congenital Amaurosis, RPE65-associated
macular corneal dystrophy Macular corneal dystrophy
Megalocornea Megalocornea
North Carolina macular dystrophy North Carolina macular dystrophy
Oculocutaneous albinism Oculocutaneous albinism
Pattern Dystrophy | New 9.18.2017 addition to existing entry
Peters anomaly with bilateral paracentral corneal opacities associated with areas of iridocorneal touch Peters anomaly
pseudoexfoliation syndrome pseudoexfoliation syndrome
Retinal hemangioblastoma associated with Von-Hippel Lindau syndrome Retinal hemangioblastoma associated with Von-Hippel Lindau syndrome
Retinitis Pigmentosa (RP) | New 9.18.2017 addition to existing entry
Riley-Day Syndrome (Familial Dysautonomia) with Neurotrophic Keratopathy Riley-Day Syndrome (Familial Dysautonomia) with Neurotrophic Keratopathy
Schnyder Corneal Dystrophy Schnyder Corneal Dystrophy
Sectoral retinitis pigmentosa Sectoral retinitis pigmentosa
Sorsby Macular dystrophy Sorsby macular dystrophy
Stargardt's disease Stargardt's Disease
Usher Syndrome Usher Syndrome


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Ophthalmic Atlas Images by EyeRounds.org, The University of Iowa are licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.

last updated: 09/25/2017
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