Purpose. To describe the first reported case of West African crystalline maculopathy (WACM) from a member of the Benin tribe and explore the association with sickle cell retinopathy. Methods. Full ophthalmic examination and high-resolution ocular coherence tomographic imaging. Patients. 61-year-old patient from an academic retina practice. Results. The patient demonstrated bilateral yellow-green birefringent crystals localized to the inner retina on optical coherence tomography, as well as sickle cell-related neovascularization in the right eye. She reported no consumption of kola nuts. Conclusions. Associated retinal vascular disease may be important in the pathogenesis of crystalline maculopathy
Tunji Sunday OluleyeRetina and Vitreous Unit, Department of Ophthalmology, University College Hospit...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Objective: The present study aims to describe ocular alterations in sickle cell disease patients in ...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
We present two patients with crystalline maculopathy seen at the Eye Clinic of the University Colleg...
We present two patients with crystalline maculopathy seen at the Eye Clinic of the University Colleg...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Bone infarction involving the orbit in sickle cell disease is not common. Bilateral orbital infarcti...
To identify systemic risk factors for sickle cell maculopathy, and to analyze the microstructure of ...
Presenting Symptom: Blurred vision OD; Cotton wool spots. Pathology: Retinal hemorrhage. Clinical: A...
A 52-year-old black man with a history of sickle cell SS disease presented with sudden loss of visio...
International audienceTo identify genetic, systemic, and biological factors associated with the occu...
Hemoglobinopathies are genetic disorders that lead to abnormal structure of the hemoglobin molecule....
Best macular dystrophy is reported to be rare in Africans. It is a hereditary disease that starts in...
Tunji Sunday OluleyeRetina and Vitreous Unit, Department of Ophthalmology, University College Hospit...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Objective: The present study aims to describe ocular alterations in sickle cell disease patients in ...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
We present two patients with crystalline maculopathy seen at the Eye Clinic of the University Colleg...
We present two patients with crystalline maculopathy seen at the Eye Clinic of the University Colleg...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Bone infarction involving the orbit in sickle cell disease is not common. Bilateral orbital infarcti...
To identify systemic risk factors for sickle cell maculopathy, and to analyze the microstructure of ...
Presenting Symptom: Blurred vision OD; Cotton wool spots. Pathology: Retinal hemorrhage. Clinical: A...
A 52-year-old black man with a history of sickle cell SS disease presented with sudden loss of visio...
International audienceTo identify genetic, systemic, and biological factors associated with the occu...
Hemoglobinopathies are genetic disorders that lead to abnormal structure of the hemoglobin molecule....
Best macular dystrophy is reported to be rare in Africans. It is a hereditary disease that starts in...
Tunji Sunday OluleyeRetina and Vitreous Unit, Department of Ophthalmology, University College Hospit...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Objective: The present study aims to describe ocular alterations in sickle cell disease patients in ...