Search results (100 results)

Nov 29 2022 by Niloofar Piri, MD

Fundus photograph of the left eye in a 58 yo male with rod cone dystrophy. He presented with night blindness and peripheral vision loss since youth and recent decrease in central vision for the past 10 years. Notice waxy pallor of the nerve, severe arterial narrowing and chorioretinal atrophy mainly around the arcades as well as posterior pole along with RPE hyperplastic changes and atrophy. RPE atrophy in midperiphery has coin shaped appearance. FAF has characteristic appearance (uploaded separately) He has one pathogenic variants of both CEP290 and PRPH2 genes.

Photographer: Sean Kelso, Saint Louis University

Condition/keywords: hereditary retinal deg, hereditary retinal dystrophy, Rod cone dystrophy

Nov 29 2022 by Niloofar Piri, MD

Fundus autofluorescence of the left eye in a 58 yo male with rod cone dystrophy. He presented with night blindness and peripheral vision loss since youth and recent decrease in central vision for the past 10 years. Notice multiple coin shaped hypoautofluorescent pacthes within central 20 degrees which are coalescing centrally. (fundus photo uploaded separately) He has one pathogenic variants of both CEP290 and PRPH2 genes.

Photographer: Sean Kelso, Saint Louis University

Condition/keywords: hereditary retinal degeneration, hereditary retinal dystrophy, rod cone dystrophy

Sep 6 2024 by Mauricio Bayram-Suverza, MD

A 65-year-old male patient reports experiencing bilateral blind spots that have gradually intensified over time. Genetic testing was unrevealing. The fundus autofluorescence image shows a hypoautofluorescent ring in the posterior pole, especially nasal to the nerve and along arcades.

Photographer: Mauricio Bayram-Suverza, Casey Eye Institute, OHSU.

Imaging device: Optos California

Condition/keywords: fundus autofluorescence (FAF), inherited retinal disease, nyctalopia, retinal dystrophy, retinitis pigmentosa

Sep 21 2022 by Zach Seim

Ultra-widefield fundus photo of a 74 year old male presenting with severe vision loss beginning at age 55. Patient sought a second opinion with our office and was diagnosed with Choroideremia. Patient denies hearing loss, heart problems, balance issues, polydactyly, kidney problems, and dental problems. Patient reports that nobody in the family had blindness. Choroideremia is an X-linked chorioretinal dystrophy characterized by the diffuse, progressive degeneration of the retinal pigment epithelium (RPE), photoreceptors and choriocapillaris. It is caused by a mutation in the CHM gene.

Photographer: Zach Seim

Imaging device: Optos California

Condition/keywords: choroideremia, hereditary choroidal atrophy, hereditary retinal dystrophy, Optos, pseudocolor, ultra-wide field imaging

Sep 21 2022 by Zach Seim

Ultra-widefield fundus photo of a 74 year old male presenting with severe vision loss beginning at age 55. Patient sought a second opinion with our office and was diagnosed with Choroideremia. Patient denies hearing loss, heart problems, balance issues, polydactyly, kidney problems, and dental problems. Patient reports that nobody in the family had blindness. Choroideremia is an X-linked chorioretinal dystrophy characterized by the diffuse, progressive degeneration of the retinal pigment epithelium (RPE), photoreceptors and choriocapillaris. It is caused by a mutation in the CHM gene.

Photographer: Zach Seim

Imaging device: Optos California

Condition/keywords: choroideremia, hereditary choroidal atrophy, hereditary retinal dystrophy, left eye, light perception, low vision, Optos, pseudocolor, ultra-wide field imaging

Jul 20 2023 by Harsh Vardhan Singh, MS

52-year-old male with a advanced stage of cone-rod dystrophy

Photographer: Harsh Vardhan Singh, AIIMS, Guwahati

Imaging device: Zeiss Clarus 700

Condition/keywords: cone dystrophy, Cone-Rod Dystrophy, pigmentary retinal dystrophy, retinal dystrophy

Nov 7 2023 by Jolee Rodriguez

Bilateral fundus photography and fundus autofluorescence imaging of a 62-year-old male with Retinitis Pigmentosa. Patient reported visual field defects and dark adapting issues. Patient's vision at the time images were taken were sc20/20 of the right eye and sc20/25 of the left eye. Dr. Sutherland determined that based on the patient's lack of family history, the most likely route of inheritance is autosomal recessive.

Photographer: Jolee Rodriguez

Imaging device: Optos California RGB

Condition/keywords: autofluorescence imaging, fundus photography, hereditary retinal dystrophy, Optos, OPTOS CALIFORNIA RGB, retinitis pigmentosa, ultra-wide field imaging, Ultra-wide field retinal imaging, ultra-widefield image

Jan 6 2019 by Hashim Ali Khan, OD, FAAO

Montage of Multiple Fundus Photographs from the right eye of a 25-year-old woman with gyrate atrophy.

Photographer: Ahmed Abbass

Imaging device: Topcon TRC-NW8F

Condition/keywords: gyrate atrophy, hereditary retinal dystrophy, retinal dystrophy

Feb 22 2018 by Nichole Lewis

Reticular Drusen, Doyne's Honeycomb Retinal Dystrophy, Malattia Leventinese, Familial Dominant Drusen

Photographer: Nichole Lewis

Condition/keywords: Doyne's Honeycomb, Familial Dominant Drusen, Malattia Leventinese, reticular drusen

Apr 14 2018 by Hamza Ahmed Shawky

Right fundus color photograph of a 35-year-old man with central areolar choroidal dystrophy, BCVA is 6/60

Photographer: Hamza Shawky, Alferdaws eye hospital, Retina unit

Imaging device: Heidelberg Spectralis

Condition/keywords: central areolar choroidal dystrophy (CACD), hereditary retinal dystrophy, macular dystrophy, retinal dystrophy

Mar 29 2019 by Jessica Norkus

Optos ultra wide field image of 41-year-old male patient with pigmentary retinal dystrophy. Atypical findings due to unilateral presentation. Patient has been experiencing symptoms for 15 years, notes significant nyctalopia.

Photographer: Jessica Norkus

Imaging device: Optos Ultra Wide Field Camera

Condition/keywords: abnormal fundus, bone spicule, color fundus photograph, color photo, fundus autofluorescence (FAF), fundus photograph, Optos, peripheral bone spicules, pigment changes, ultra-wide field imaging, unilateral blindness

Mar 29 2019 by Jessica Norkus

Optos ultra wide field image of 41-year-old male patient with pigmentary retinal dystrophy. Atypical findings due to unilateral presentation. Patient has been experiencing symptoms for 15 years, notes significant nyctalopia.

Photographer: Jessica Norkus

Imaging device: Optos Ultra Wide Field Camera

Condition/keywords: abnormal fundus, bone spicule, color fundus photograph, color photo, fundus photograph, Optos, peripheral bone spicules, pigment changes, ultra-wide field imaging, unilateral blindness

Sep 19 2022 by Kenneth Fong

34 year old male with colour blindness and loss of visual field

Condition/keywords: retinal dystrophy

Apr 14 2018 by Hamza Ahmed Shawky

Left fundus autofluorescence photograph of a 35-year-old man with central areolar choroidal dystrophy, BCVA is 6/60

Photographer: Hamza Shawky, Alferdaws eye hospital, Retina unit

Imaging device: Heidelberg Spectralis

Condition/keywords: central areolar choroidal dystrophy (CACD), hereditary retinal dystrophy, macular dystrophy, retinal dystrophy

Apr 14 2018 by Hamza Ahmed Shawky

Right fundus OCT of a 35-year-old man with central areolar choroidal dystrophy, BCVA is 6/60

Photographer: Hamza Shawky, Alferdaws eye hospital, Retina unit

Imaging device: Heidelberg Spectralis

Condition/keywords: central areolar choroidal dystrophy (CACD), hereditary retinal dystrophy, macular dystrophy, retinal dystrophy

Apr 14 2018 by Hamza Ahmed Shawky

Right fundus autofluorescence photograph of a 35-year-old man with central areolar choroidal dystrophy, BCVA is 6/60

Photographer: Hamza Shawky, Alferdaws eye hospital, Retina unit

Imaging device: Heidelberg Spectralis

Condition/keywords: central areolar choroidal dystrophy (CACD), hereditary retinal dystrophy, macular dystrophy, retinal dystrophy

Dec 9 2024 by Mauricio Bayram-Suverza, MD

A 54 year-old male patient presented with asteroid hyalosis. Retinal examination revealed the presence of bone spicules, primarily located in the mid-periphery. Genetic testing identified a pathogenic variant in the RHO gene.

Photographer: Mauricio Bayram-Suverza, Casey Eye Institute, OHSU.

Imaging device: Optos California

Condition/keywords: Asteroid hyalosis, retinal dystrophy, Retinitis Pigmentosa, vitreous

Feb 27 2025 by Daniel Davis, OCT-C

Color fundus photo of 55-year-old female with Astrocytic Hamartoma in association with tuberous sclerosis. No treatment options available, benign. Other findings include; Posterior Vitreous Detachment, Vitreous Hemorrhage, Hereditary Retinal Dystrophy, Vitreous Opacities, Hypertensive Retinopathy.

Photographer: Daniel Davis, OCT-C

Imaging device: Optos California

Condition/keywords: color fundus photograph

Feb 27 2025 by Daniel Davis, OCT-C

Fundus autofluorescence photo of 55-year-old female with astrocytic hamartoma in association with tuberous sclerosis. No treatment options available, benign. Other findings include; Posterior Vitreous Detachment, Vitreous Hemorrhage, Hereditary Retinal Dystrophy, Vitreous Opacities, Hypertensive Retinopathy.

Photographer: Daniel Davis, OCT-C

Imaging device: Optos California

Condition/keywords: astrocytic hamartoma, fundus autofluorescence (FAF)

Jan 15 2019 by Olivia Rainey

Ultra-wide field fluorescein angiogram of an 85-year-old female with a branch retinal vein occlusion with peripheral pigmentary changes. Patient developed a BRVO after a PPV for an epiretinal membrane.

Photographer: Olivia Rainey

Imaging device: Optos

Condition/keywords: branch retinal vein occlusion (BRVO), epiretinal membrane (ERM), fluorescein angiogram (FA), left eye, Optos, pigmentary retinal dystrophy

Apr 14 2018 by Hamza Ahmed Shawky

Right fundus late FFA photograph of a 35-year-old man with central areolar choroidal dystrophy, BCVA is 6/60

Photographer: Hamza Shawky, Alferdaws eye hospital, Retina unit

Imaging device: Heidelberg Spectralis

Condition/keywords: central areolar choroidal dystrophy (CACD), hereditary retinal dystrophy, macular dystrophy, retinal dystrophy

Apr 14 2018 by Hamza Ahmed Shawky

Left fundus smartphone photograph of a 35-year-old man with central areolar choroidal dystrophy, BCVA is 6/60

Photographer: Hamza Shawky, Alferdaws eye hospital, Retina unit

Imaging device: smartphone fundus photography

Condition/keywords: central areolar choroidal dystrophy (CACD), hereditary retinal dystrophy, macular dystrophy, retinal dystrophy

Apr 14 2018 by Hamza Ahmed Shawky

Right fundus smartphone photograph of a 35-year-old man with central areolar choroidal dystrophy, BCVA is 6/60

Photographer: Hamza Shawky, Alferdaws eye hospital, Retina unit

Imaging device: smartphone fundus photography

Condition/keywords: central areolar choroidal dystrophy (CACD), hereditary retinal dystrophy, macular dystrophy, retinal dystrophy

Apr 14 2018 by Hamza Ahmed Shawky

Left fundus OCT of a 35-year-old man with central areolar choroidal dystrophy, BCVA is 6/60

Photographer: Hamza Shawky, Alferdaws eye hospital, Retina unit

Imaging device: Heidelberg Spectralis

Condition/keywords: central areolar choroidal dystrophy (CACD), hereditary retinal dystrophy, macular dystrophy, retinal dystrophy

Apr 14 2018 by Hamza Ahmed Shawky

Left fundus color photograph of a 35-year-old man with central areolar choroidal dystrophy, BCVA is 6/60.

Photographer: Hamza Shawky, Alferdaws eye hospital, Retina unit

Imaging device: Heidelberg Spectralis

Condition/keywords: central areolar choroidal dystrophy (CACD), hereditary retinal dystrophy, macular dystrophy, retinal dystrophy