Add to ORKGSickle-cell disease is characterized by recurrent vascular occlusive episodes and a progressive obliteration of capillary beds. This process can be directly observed in the eye and its occurrence in the peripheral retina has been well documented (Welch and Goldberg, I966; Goldberg, 1971
O presente estudo teve como objetivo descrever as alterações oculares em pacientes portadores de doe...
Abstract: Sickle cell disease is hereditary hemoglobinopathy which causes haemolytic anemia, vaso-oc...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Sickle cell hemoglobinopathies all share the common feature of an abnormal globin chain, which leads...
Objective: The present study aims to describe ocular alterations in sickle cell disease patients in ...
Summary Hemoglobinopathies are a group of hereditary diseases that cause quantitative or qualitative...
The World Health Organization counts that more than 5% of the world's population carry some type of ...
Presenting Symptom: Occluded retinal artery. Pathology: Retinal artery occlusion. Clinical: The pati...
p. 259-263.OBJECTIVE: The present study aims to describe ocular alterations in sickle cell disease p...
tObjective: The aim of the present study was to characterize sickle cell disease retinopathyin child...
Presenting Symptom: Blurred vision OD; Cotton wool spots. Pathology: Retinal hemorrhage. Clinical: A...
A patient with red eyes and ocular deconges-tants drops (tetrahidrozolyne 0.05%) use his-tory, was o...
Hemoglobinopathies are genetic disorders that lead to abnormal structure of the hemoglobin molecule....
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Objective: The aim of the present study was to characterize sickle cell disease retinopathy in child...
O presente estudo teve como objetivo descrever as alterações oculares em pacientes portadores de doe...
Abstract: Sickle cell disease is hereditary hemoglobinopathy which causes haemolytic anemia, vaso-oc...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Sickle cell hemoglobinopathies all share the common feature of an abnormal globin chain, which leads...
Objective: The present study aims to describe ocular alterations in sickle cell disease patients in ...
Summary Hemoglobinopathies are a group of hereditary diseases that cause quantitative or qualitative...
The World Health Organization counts that more than 5% of the world's population carry some type of ...
Presenting Symptom: Occluded retinal artery. Pathology: Retinal artery occlusion. Clinical: The pati...
p. 259-263.OBJECTIVE: The present study aims to describe ocular alterations in sickle cell disease p...
tObjective: The aim of the present study was to characterize sickle cell disease retinopathyin child...
Presenting Symptom: Blurred vision OD; Cotton wool spots. Pathology: Retinal hemorrhage. Clinical: A...
A patient with red eyes and ocular deconges-tants drops (tetrahidrozolyne 0.05%) use his-tory, was o...
Hemoglobinopathies are genetic disorders that lead to abnormal structure of the hemoglobin molecule....
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...
Objective: The aim of the present study was to characterize sickle cell disease retinopathy in child...
O presente estudo teve como objetivo descrever as alterações oculares em pacientes portadores de doe...
Abstract: Sickle cell disease is hereditary hemoglobinopathy which causes haemolytic anemia, vaso-oc...
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (S...