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- W2001748466 abstract "Hemoglobinopathies are a group of inherited disorders characterized by quantitative or qualitative malformations of hemoglobin (Hb). Some of these diseases present vaso-occlusive phenomena that are responsible for high morbidity in clinical and/or ophthalmologic terms. Diagnosis of hemoglobinopathies is performed exclusively through hemoglobin electrophoresis. From the ophthalmologic perspective, the most important representative of this group of diseases is sickle cell retinopathy, which presents a wide spectrum of fundus manifestations and may even lead to irreversible vision loss if not properly diagnosed and treated. The aim of this review is to present the classification of sickle cell retinopathy and to describe current management and future perspectives for its treatment, taking into consideration the clinical management of these patients." @default.
- W2001748466 created "2016-06-24" @default.
- W2001748466 creator A5009693209 @default.
- W2001748466 creator A5039584200 @default.
- W2001748466 date "2013-10-01" @default.
- W2001748466 modified "2023-09-23" @default.
- W2001748466 title "Sickle cell retinopathy: diagnosis and treatment" @default.
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- W2001748466 doi "https://doi.org/10.1590/s0004-27492013000500016" @default.
- W2001748466 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24232951" @default.
- W2001748466 hasPublicationYear "2013" @default.
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